Filed Pursuant to Rule 424(b)(5)
Registration No. 333-274083
(To the Prospectus Dated August 28, 2023)
15,000,000 Shares of Class A Common Stock |
|
Pre-funded Warrants to Purchase up to 6,000,000 Shares of Class A Common Stock |
Warrants to Purchase up to 10,500,000 Shares of Class A Common Stock |
BioVie Inc.
We are offering 15,000,000 shares (the “Shares”) of our
Class A common stock, $0.0001 par value per share (the “Common Stock”), at an offering price of $1.00 per Share, pursuant
to this prospectus supplement and the accompanying base prospectus.
We are also offering pre-funded warrants to purchase up to 6,000,000 shares of Common
Stock (“Pre-funded Warrants”) in lieu of shares of Common Stock, exercisable at an exercise price of $0.0001 per share. The
purchase price of each Pre-funded Warrant is equal to $0.9999. The Pre-funded Warrants will be immediately exercisable and may be exercised
at any time until all of the Pre-funded Warrants are exercised in full.
The Shares and Pre-funded Warrants are being sold together with warrants to purchase up
to 10,500,000 shares of our Common Stock (the “Common Warrants”). Each Common Warrant has an exercise price per share of $1.50,
will be exercisable immediately and will expire on the fifth anniversary of the original issuance date.
The Shares, Pre-funded Warrants and Common Warrants
can only be purchased together in this offering but will be issued separately and will be immediately separable upon issuance.
We have engaged ThinkEquity LLC (the “placement agent”) to act as our exclusive placement agent in connection with this offering. The placement agent has agreed to use its reasonable
best efforts to arrange for the sale of the securities offered by this prospectus. The placement agent is not purchasing or selling any
of the securities we are offering and the placement agent is not required to arrange the purchase or sale of any specific number or dollar
amount of securities. We have agreed to pay placement agent fees to the placement agent as set forth in the table below, which assumes
that we sell all of the securities offered by this prospectus. Since we will deliver the securities to be issued in this offering upon
our receipt of investor funds, there is no arrangement for funds to be received in escrow, trust or similar arrangement. There is no minimum
offering requirement as a condition of closing of this offering. Because there is no minimum offering amount required as a condition to
closing this offering, we may sell fewer than all of the securities offered hereby, which may significantly reduce the amount of proceeds
received by us, and investors in this offering will not receive a refund in the event that we do not sell an amount of securities sufficient
to pursue our business goals described in this prospectus. In addition, because there is no escrow account and no minimum offering amount,
investors could be in a position where they have invested in our company, but we are unable to fulfill all of our contemplated objectives
due to a lack of interest in this offering. Further, any proceeds from the sale of securities offered by us will be available for our
immediate use, despite uncertainty about whether we would be able to use such funds to effectively implement our business plan. See the
section entitled “Risk Factors” for more information. We will bear all costs associated with the offering. See “Plan
of Distribution” on page S-31 of this prospectus for more information regarding
these arrangements.
Our Common Stock is traded on The Nasdaq Capital Market under the symbol “BIVI.” On February
29, 2024, the closing price for our Common Stock, as reported on The Nasdaq Capital Market was $1.24 per share. There is no established
trading market for the Pre-funded Warrants or the Common Warrants, and we do not intend to list the Pre-funded Warrants or the Common
Warrants on any securities exchange or nationally recognized trading system.
Investing in these securities involves certain
risks. See “Risk Factors” on page S-6 of this prospectus supplement and the accompanying base prospectus, as well as the
risk factors incorporated by reference into this prospectus supplement and accompanying base prospectus for a discussion of the factors
you should carefully consider before deciding to purchase these securities.
Neither the Securities and Exchange Commission
nor any state securities commission has approved or disapproved of these securities or determined if this prospectus supplement or accompanying
base prospectus is truthful or complete. Any representation to the contrary is a criminal offense.
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Per Share of Common Stock and
Accompanying Common Warrant |
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Per Pre-funded Warrant and
accompanying Common Warrant |
|
|
Total(2) |
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Public offering price |
|
$ |
1.000 |
|
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$ |
0.9999 |
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$ |
21,000,000 |
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Placement agent fees (1) |
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$ |
0.075 |
|
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$ |
0.7499 |
|
|
$ |
1,575,000 |
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Proceeds to us, before expenses |
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$ |
0.925 |
|
|
$ |
0.9249 |
|
|
$ |
19,425,000 |
|
|
(1) |
Does not include a non-accountable expense allowance of 1% of the gross proceeds. See “Plan of Distribution” beginning on page S-31 of this prospectus supplement for additional information regarding placement agent fees and estimated expenses. |
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(2) |
Based on the sale of 15,000,000 shares of Common Stock, 6,000,000 Pre-funded Warrants, and 10,500,000
Common Warrants and assuming full exercise of the Pre-funded Warrants. |
The delivery to purchasers of the Shares, Pre-funded
Warrants, and the Common Warrants offered and sold in this offering is expected to be made on or about March 6, 2024, subject to satisfaction
of certain customary closing conditions.
ThinkEquity
The date of this prospectus supplement is March 4,
2024
TABLE OF CONTENTS
PROSPECTUS SUPPLEMENT
PROSPECTUS
ABOUT THIS PROSPECTUS SUPPLEMENT
This prospectus supplement and the accompanying base
prospectus are part of a registration statement on Form S-3 (File No. 333-274083) that we filed with the Securities and Exchange Commission
(the “SEC”) on August 18, 2023, and that was declared effective by the SEC on August 28, 2023 using a “shelf”
registration process. This document is in two parts. The first part is this prospectus supplement, which describes the specific terms
of this offering and also adds to and updates information contained in the accompanying base prospectus and the documents incorporated
by reference herein. The second part, the accompanying base prospectus, provides more general information, some of which may not apply
to this offering. Generally, when we refer to this prospectus, we are referring to both the prospectus supplement and the accompanying
base prospectus combined. To the extent there is a conflict between the information contained in this prospectus supplement and the information
contained in the accompanying base prospectus or any document incorporated by reference therein filed prior to the date of this prospectus
supplement, you should rely on the information in this prospectus supplement. If any statement in one of these documents is inconsistent
with a statement in another document having a later date—for example, a document incorporated by reference in the accompanying base
prospectus—the statement in the document having the later date modifies or supersedes the earlier statement.
We further note that the representations, warranties
and covenants made by us in any agreement that is filed as an exhibit to any document that is incorporated by reference herein were made
solely for the benefit of the parties to such agreement, including, in some cases, for the purpose of allocating risk among the parties
to such agreements, and should not be deemed to be a representation, warranty or covenant to you. Moreover, such representations, warranties
or covenants were accurate only as of the date when made. Accordingly, such representations, warranties and covenants should not be relied
on as accurately representing the current state of our affairs.
You should rely only on the information contained in this prospectus supplement or the accompanying
base prospectus or incorporated by reference herein or therein. We have not authorized, and the placement agent has not authorized, anyone
to provide you with information that is different. The information contained in this prospectus supplement or the accompanying base prospectus
or incorporated by reference herein or therein is accurate only as of the respective dates thereof, regardless of the time of delivery
of this prospectus supplement and the accompanying base prospectus or of any sale of our securities.
This prospectus supplement and the accompanying base
prospectus contain summaries of certain provisions contained in some of the documents described herein, but reference is made to the actual
documents for complete information. All of the summaries are qualified in their entirety by the actual documents. Copies of some of the
documents referred to herein have been filed, will be filed or will be incorporated herein by reference as exhibits to the registration
statement, and you may obtain copies of those documents as described below in the section entitled “Where You Can Find More Information.”
It is important for you to read and consider all information
contained in this prospectus supplement and the accompanying base prospectus, including the documents incorporated by reference herein
and therein, in making your investment decision. You should also read and consider the information in the documents to which we have referred
you in the sections entitled “Where You Can Find More Information” and “Incorporation of Certain Information By Reference”
in this prospectus supplement and in the accompanying base prospectus, respectively.
This prospectus supplement and the accompanying base
prospectus contain and incorporate by reference market data and industry statistics and forecasts that are based on independent industry
publications and other publicly-available information. Although we believe these sources are reliable, we do not guarantee the accuracy
or completeness of this information and we have not independently verified this information. Although we are not aware of any misstatements
regarding the market and industry data presented in this prospectus supplement, accompanying base prospectus or the documents incorporated
herein by reference, these estimates involve risks and uncertainties and are subject to change based on various factors, including those
discussed in the section entitled “Risk Factors” in this prospectus supplement and the accompanying base prospectus, and under
similar headings in the other documents that are incorporated by reference herein and therein. Accordingly, investors should not place
undue reliance on this information.
We are offering to sell, and seeking offers to buy,
the securities offered by this prospectus supplement only in jurisdictions where offers and sales are permitted. The distribution of this
prospectus supplement and the accompanying base prospectus and the offering of the securities offered by this prospectus supplement in
certain jurisdictions may be restricted by law. Persons outside the United States who come into possession of this prospectus supplement
and the accompanying base prospectus must inform themselves about, and observe any restrictions relating to, the offering of the securities
and the distribution of this prospectus supplement and the accompanying base prospectus outside the United States. This prospectus supplement
and the accompanying base prospectus do not constitute, and may not be used in connection with, an offer to sell, or a solicitation of
an offer to buy, any securities offered by this prospectus supplement and the accompanying base prospectus by any person in any jurisdiction
in which it is unlawful for such person to make such an offer or solicitation.
Unless the context otherwise indicates, references
in this prospectus to, “BioVie,” “the Company,” “we,” “our,” or “us” mean
BioVie Inc., a Nevada corporation.
PROSPECTUS SUPPLEMENT SUMMARY
This summary highlights certain information
about us and certain information contained elsewhere in this prospectus supplement, in the accompanying base prospectus and in the
documents incorporated by reference herein and therein. This summary is not complete and does not contain all of the information
that you should consider before making an investment decision. For a more complete understanding of the Company, you should read and
consider carefully the more detailed information included in this prospectus supplement and the accompanying base prospectus, ,
including the factors described under the heading “Risk Factors,” on page S-6 of this prospectus supplement, the
“Risk Factors” section beginning on page 5 of the accompanying base prospectus as well as the information incorporated
herein and therein by reference, before making an investment decision.
Overview of the Company
We are a clinical-stage company developing innovative
drug therapies to treat chronic debilitating conditions including liver disease and neurological and neuro-degenerative disorders.
Neurodegenerative Disease Program
In neurodegenerative disease, the Company’s
drug candidate NE3107 inhibits activation of inflammatory actions extracellular single-regulated kinase (“ERK”) and nuclear
factor kappa-light-chain-enhancer of activated B cells (“NFκB”) (including interactions with tumor necrosis factor (“TNF”)
signaling and other relevant inflammatory pathways) that lead to neuroinflammation and insulin resistance. NE3107 does not interfere with
their homeostatic functions (e.g., insulin signaling and neuron growth and survival). Both inflammation and insulin resistance are drivers
of Alzheimer’s disease (“AD”) and Parkinson’s disease (“PD”).
The Company acquired the
biopharmaceutical assets of NeurMedix, Inc. (“NeurMedix”) a privately held clinical-stage pharmaceutical company and a related
party in June 2021. The acquired assets included NE3107. NE3107 is an investigational, novel, orally administered small molecule
that is thought to inhibit inflammation-driven insulin resistance and major pathological inflammatory cascades with a novel mechanism
of action. There is emerging scientific consensus that both inflammation and insulin resistance may play fundamental roles in the development
of AD and PD, and NE3107 could, if approved by FDA, represent an entirely new medical approach to treating these devastating conditions
affecting an estimated 6 million Americans suffering from AD and 1 million Americans suffering from PD.
A. Alzheimer’s Disease
(NCT05083260)
On November 29, 2023, the
Company announced the analysis of its unblinded, topline efficacy data from its Phase 3 clinical trial (NCT04669028) of NE3107 in the
treatment of mild to moderate AD. The study has co-primary endpoints looking at cognition using the Alzheimer’s Disease Assessment
Scale-Cognitive Scale (ADAS-Cog 12) and function using the Clinical Dementia Rating-Sum of Boxes (CDR-SB). Patients were randomly assigned,
1:1 versus placebo, to receive sequentially 5 mg of NE3107 orally twice a day for 14 days, then 10 mg orally twice a day for 14 days,
followed by 26 weeks of 20 mg orally twice daily.
Upon trial completion, as the Company began the process
of unblinding the trial data, the Company found significant deviation from protocol and current good clinical practices (“cGCPs”)
violations at 15 study sites (virtually all of which were from one geographic area). This highly unusual level of suspected improprieties
led the Company to exclude all patients from these sites and to refer the sites to the U.S. Food and Drug Administration (“FDA”)
Office of Scientific Investigations (“OSI”) for further action. After the patient exclusions and other exclusions per the
statistical analysis plan, only 57 patients remained in the Per-Protocol population, which included those who completed the trial and
were verified to take study drug from pharmacokinetic data.
The trial was originally designed to be 80% powered
with 125 patients in each of the treatment and placebo arms. The unplanned exclusion of so many patients has left the trial unpowered
for the primary endpoints.
In the Per-Protocol population, which included those
patients who completed the trial and who were further verified to have taken the study drug (based on pharmacokinetic data), an observed
descriptive change from baseline appeared to suggest a slowing of cognitive loss; these same patients experienced an advantage in age
deceleration vs. placebo as measured by DNA epigenetic change. Age deceleration is used by longevity researchers to measure the difference
between the patient’s biological age, in this case as measured by the Horvath DNA methylation Skin Blood Clock, relative to the
patient’s actual chronological age. This test was a non-primary/secondary endpoint, other-outcome measure, done via blood test collected
at week 30 (end of study). Additional DNA methylation data continues to be collected and analyzed.
Based on the efficacy signal seen in this trial, the
Company is exploring (1) a discussion with the FDA to potentially employ the adaptive trial feature of the protocol to continue enrolling
patients to achieve statistical significance; and/or (2) designing a new Phase 3 study of NE3107 that leverages the most recent data and
understanding of the potential effect NE3017 may have in helping persons with AD.
B. Parkinson’s Disease
(NCT05083260)
The Phase 2 study of NE3107
for the treatment of PD (NCT05083260), completed in January 2023, was a double-blind, placebo-controlled, safety, tolerability, and pharmacokinetics
study in PD participants treated with carbidopa/levodopa and NE3107. Forty-five patients with a defined L-dopa “off state”
were randomized 1:1 to placebo:NE3107 20 mg twice daily for 28 days. This trial was launched with two design objectives: (1) the primary
objective was safety and a drug-drug interaction study as requested by the FDA to measure the potential for adverse interactions of NE3107
with carbidopa/ levodopa; and (2) the secondary objective was to determine if preclinical indications of promotoric activity and apparent
enhancement of levodopa activity could be seen in humans. Both objectives were met.
C. NE3017 Synopsis
Neuroinflammation, insulin
resistance, and oxidative stress are common features in the major neurodegenerative diseases, including AD, PD, frontotemporal lobar dementia,
and Amyotrophic lateral sclerosis. NE3107 is an investigational oral small molecule, blood-brain permeable, compound with potential anti-inflammatory,
insulin sensitizing, and ERK-binding properties that may allow it to selectively inhibit ERK-, NFκB- and TNF-stimulated inflammation.
NE3107’s potential to inhibit neuroinflammation and insulin resistance forms the basis for the Company’s work testing the
molecule in AD and PD patients. NE3107 is patented in the United States, Australia, Canada, Europe and South Korea.
Liver Disease Program
In liver disease, our investigational drug candidate
BIV201 (continuous infusion terlipressin), which has been granted both FDA Fast Track designation status and FDA Orphan Drug status, is
being evaluated and discussed after receiving guidance from the FDA regarding the design of Phase 3 clinical testing of BIV201 for the
treatment of ascites due to chronic liver cirrhosis. BIV201 is administered as a patent-pending liquid formulation.
In June 2021, the Company initiated a Phase 2 study
(NCT04112199) designed to evaluate the efficacy of BIV201 (terlipressin, administered by continuous infusion for two 28-day treatment
cycles) combined with standard-of-care (“SOC”), compared to SOC alone, for the treatment of refractory ascites. The primary
endpoints of the study are the incidence of ascites-related complications and change in ascites fluid accumulation during treatment compared
to a pre-treatment period.
In March 2023, the Company announced enrollment was
paused and that data from the first 15 patients treated with BIV201 plus SOC appeared to show at least a 30% reduction in ascites fluid
during the 28 days after treatment initiation compared to the 28 days prior to treatment. The change in ascites volume was significantly
different from those patients receiving SOC treatment. Patients who completed the treatment with BIV201 experienced a 53% reduction in
ascites fluid, which was sustained (43% reduction) during the three months after treatment initiation as compared to the three-month pre-treatment
period.
In June 2023, the Company requested and subsequently
received guidance from the FDA regarding the design and endpoints for definitive clinical testing of BIV201 for the treatment of ascites
due to chronic liver cirrhosis. The Company is currently finalizing protocol designs for the Phase 3 study of BIV201 for the treatment
of ascites due to chronic liver cirrhosis.
While the active agent, terlipressin, is approved
in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis, treatment of ascites is not included in these
authorizations. Patients with refractory ascites suffer from frequent life-threatening complications, generate more than $5 billion in
annual treatment costs, and have an estimated 50% mortality rate within 6 to 12 months. The U.S. FDA has not approved any drug to treat
refractory ascites.
The BIV201 development program was initiated by LAT
Pharma LLC. On April 11, 2016, the Company acquired LAT Pharma LLC and the rights to its BIV201 development program. The Company currently
owns all development and marketing rights to this drug candidate. Pursuant to the Agreement and Plan of Merger entered into on April 11,
2016, between our predecessor entities, LAT Pharma LLC and NanoAntibiotics, Inc., BioVie is obligated to pay a low single digit royalty
on net sales of BIV201 (continuous infusion terlipressin) to be shared among LAT Pharma Members, PharmaIn Corporation, and The Barrett
Edge, Inc.
Corporate Information
Our principal executive office is located at 680 W.
Nye Lane, Suite 201, Carson City, Nevada 89703, and our phone number is (775) 888-3162.
THE OFFERING
Common Stock offered by us |
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15,000,000 shares of our Common Stock. |
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Pre-funded Warrants Offered |
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We are also
offering Pre-funded Warrant to purchase up to 6,000,000 shares of our Common Stock, exercisable at an exercise price of $0.0001 per share
to those purchasers whose purchase of the Common Stock in this offering would result in the purchaser, together with its affiliates and
certain related parties, beneficially owning more than 4.99% (or at the election of the purchaser, 9.99%) of our outstanding Common Stock
immediately following the consummation of this offering.
The purchase price of each Pre-funded Warrant is $0.9999. The Pre-funded
Warrants are immediately exercisable and may be exercised at any time until all of the Pre-funded Warrants are exercised in full.
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Common Warrants Offered |
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We are also offering Common Warrants to purchase an
aggregate of 10,500,000 shares of our Common Stock. The Shares and the Pre-funded Warrant are being sold together with the Common Warrants.
Each Common Warrant has an exercise price per share of $1.50, will be exercisable immediately and will expire on the fifth anniversary
of the original issuance date.
This prospectus also relates to the offering of the
shares of Common Stock issuable upon exercise of the Common Warrants.
For additional information regarding the terms of
the Common Warrants, see “Description of Securities We Are Offering.” |
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Public Offering Price |
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$1.00 per share of Common Stock ($0.9999 per Pre-funded Warrant). |
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Common Stock outstanding following this Offering |
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60,924,596 shares of Common Stock, assuming the full exercise of the
Pre-funded Warrants and none of the Common Warrants. |
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Use of Proceeds |
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We estimate that our net proceeds from this offering will be approximately $19.0 million, after
deducting the placement agent fees and estimated offering expenses payable by us, and excluding the proceeds, if any, from the exercise
of the Common Warrants in this offering.
We intend to use the net proceeds from this offering
for working capital and general corporate purposes. See “Use of Proceeds” for a more complete description of the intended
use of proceeds from this offering. |
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Lock-Up Agreements |
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Our executive officers, directors, and certain holders of 5% or more of our Common Stock have agreed with the placement agent not to sell, transfer or dispose of any shares or similar securities for a period of 90 days from the date of this prospectus supplement. |
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Dividend Policy |
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We have never declared or paid cash dividends on our Common Stock and do not anticipate paying any cash dividends in the foreseeable future but intend to retain our capital resources for reinvestment in our business. |
Trading Market and Ticker Symbol for Common Stock |
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Our Common Stock is listed on The Nasdaq Capital Market
under the symbol “BIVI.”
There is no established trading market for the Pre-funded Warrants or Common Warrants, and we do not expect a trading
market to develop. We do not intend to list the Pre-funded Warrants or Common Warrants on any securities exchange or nationally recognized
trading system. |
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Risk Factors |
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Investing in our securities involves a high degree of risk. For a discussion of factors to consider before deciding to invest in our Common Stock, you should carefully review and consider the “Risk Factors” section beginning on page S-6 of this prospectus supplement and in the documents incorporated by reference in this prospectus supplement. |
The number of shares of Common Stock to be outstanding immediately after this offering is based
on 39,924,596 shares of our Common Stock outstanding as of February 29, 2024, and excludes:
| · | 4,169,325 shares of Common Stock issuable upon the exercise of outstanding stock options at a weighted average exercise price of $6.84
per share; |
| · | 7,770,285 shares of Common Stock issuable upon the exercise of outstanding and exercisable warrants
at a weighted average exercise price of $2.06 per share (which weighted average exercise price decreases to $1.29 per share as a result
of the adjustment to the exercise price of the Acuitas Warrants (as defined below) following this offering (See “Risk Factors –
You may experience future dilution as a result of future equity offerings or if we issue shares subject to options, warrants, stock awards
or other arrangements.”); |
| · | 585,595 shares of Common Stock issuable upon vesting of restricted stock units issued under our equity incentive plan; |
| · | 4,384 shares of Common Stock issued pursuant to the Controlled Equity Offering Sales Agreement (the “ATM Agreement”),
dated as of August 31, 2022, between the Company and Cantor Fitzgerald & Co. (the “Cantor”) since December 31, 2023; |
| · | 1,050,000 shares of Common Stock issuable upon exercise of the Placement Agent Warrants (as
defined below); and |
| · | 10,500,000 shares of Common Stock issuable upon exercise of the Common
Warrants. |
Unless otherwise indicated, this prospectus reflects
and assumes the following:
| · | no exercise of outstanding options or warrants; |
| · | no exercise of the Common Warrants issued and sold in this offering; and
|
| · | no exercise of the Placement Agent Warrants to be issued upon
consummation of this offering at an exercise price equal to 125% of the offering price of the Common Stock. |
RISK FACTORS
Investing in our securities involves a high degree
of risk. Before deciding whether to invest in our securities, you should consider carefully the risks and uncertainties discussed under
the sections titled “Risk Factors” contained in our most recent Annual Report on Form 10-K and in any subsequently filed Quarterly
Report on Form 10-Q, as well as any amendments thereto reflected in our subsequent filings with the SEC, which are incorporated by reference
into this prospectus supplement, together with other information in this prospectus supplement, the documents incorporated by reference
herein, and any prospectus supplement and any free writing prospectus that we may authorize. Please also read carefully the section titled
“Cautionary Note Regarding Forward-Looking Statements.” Additional risks and uncertainties not presently known to us, or that
we currently deem immaterial, may also adversely affect our business. In addition, past financial performance may not be a reliable indicator
of future performance and historical trends should not be used to anticipate results or trends in future periods.
Risks Relating to Our
Business and Industry
We rely and will continue
to rely on third parties to conduct our clinical trials. If these third parties do not successfully carry out their contractual duties
and/or meet expected deadlines and/or do not successfully perform and comply with regulatory requirements, including but not limited to,
the U.S. Food, Drug, and Cosmetics Act (the “FDCA”) and FDA’s implementing regulations, we may not be able to obtain
regulatory approval of or commercialize our product candidates.
We depend,
and will continue to depend, on third parties, including, but not limited to, CROs, clinical trial sites and clinical trial principal
investigators, contract laboratories, institutional review boards (“IRBs”), manufacturers, suppliers, and other third parties
to conduct our clinical trials, including those for our drug candidates NE3107 and BIV201. We rely heavily on these third parties over
the course of our clinical trials, and we control only certain aspects of their activities. Nevertheless, we retain ultimate responsibility
for ensuring that each of our studies is conducted in accordance with the protocol and applicable legal, regulatory, and scientific standards
and regulations, and our reliance on third parties does not relieve us of our regulatory responsibilities. We and these third parties
are required to comply with cGCPs, which are regulations and guidelines enforced by the FDA and comparable foreign regulatory authorities
for the conduct of clinical trials on product candidates in clinical development. Regulatory authorities enforce cGCPs through periodic
inspections and for-cause inspections of clinical trial principal investigators and trial sites. If, due to the failure of either the
Company or a third party, a clinical trial fails to comply with applicable cGCPs, FDA’s Investigational New Drug (“IND”)
requirements, other applicable regulatory requirements, or requirements set forth in the applicable IRB-approved protocol, including failure
to enroll a sufficient number of patients, the Company may be required to conduct additional clinical trials to support our marketing
applications, which would delay the regulatory approval process. Moreover, our business may be implicated if any of these third parties
violates applicable federal, state, or foreign laws and/or regulations, including but not limited to FDA’s IND regulations, fraud
and abuse or false claims laws, healthcare privacy and data security laws, or provide us or government agencies with inaccurate, misleading,
or incomplete data. For example, during routine monitoring of blinded data from our Phase 3 study (NCT04669028) of NE3107, we uncovered
what appears to be potential scientific misconduct and significant deviation from study protocol and GCP violations at fifteen sites,
which resulted in the Company excluding all patients from these sites and referring them to the FDA’s OSI for further action. The unplanned exclusion of so many patients left our Phase 3 study under
powered for the primary endpoints. These findings of potential scientific misconduct, significant deviation from protocol and GCP violations
may call into question the rigor, robustness and validity of the entire data set for this study (NCT04669028).
Although
we design the clinical trials for our product candidates, our CROs are tasked with facilitating and monitoring our clinical trials. As
a result, many important aspects of our clinical development programs, including site and investigator selection, and the conduct, timing,
and monitoring of the study, is often outside our direct control, either partially or in whole. Our reliance on third parties to conduct
clinical trials also results in less direct control over the collection, management, and quality of data developed through clinical trials
than would be the case if we were relying entirely upon our own employees. Communicating with third parties can also be challenging, potentially
leading to mistakes as well as difficulties in coordinating activities.
Risks Relating to This Offering
You may experience immediate and substantial
dilution in the net tangible book value per share of the Common Stock you purchase in the offering.
The offering price per share in this offering may exceed the net tangible book value
per share of our Common Stock outstanding prior to this offering. After giving effect to the sale by us of the Shares and accompanying
Common Warrants at a price of $1.00 per Share and Pre-funded Warrants and accompanying Common Warrants at a price of $0.9999
per Pre-funded Warrant, and after placement agent fees and estimated offering expenses payable by us and assuming full exercise of the
Pre-funded Warrants, you will experience immediate dilution of $0.58 per share, representing the difference between our net tangible book
value per share as of December 31, 2023, after giving effect to this offering and the assumed offering price. The exercise of outstanding
warrants and stock options may also result in further dilution of your investment. See the section entitled “Dilution” on
page S-30 below for a more detailed illustration of the dilution you may incur if you participate in this offering.
Our management will have broad discretion over
the use of the net proceeds from this offering, may invest or spend the proceeds raised in this offering in ways with which you may not
agree and the proceeds may not yield a significant return.
Our management will have broad discretion over the
use of proceeds from this offering. We currently intend to use the net proceeds of this offering as described in the section entitled
“Use of Proceeds.” However, our management will have broad discretion in the application of the net proceeds from this offering
and could use them for purposes other than those contemplated at the time of this offering. Accordingly, you are relying on the judgment
of our management with regard to the use of these net proceeds, and you will not have the opportunity, as part of your investment decision,
to assess whether the proceeds will be used appropriately. The failure by management to apply these funds effectively could result in
financial losses that could have a material adverse effect on our business, cause the price of our Common Stock to decline, and delay
the development of our product candidates. Pending their use, we may invest the net proceeds from this offering in short-term, interest-bearing
instruments. These investments may not yield a favorable return, or any return, to us or our stockholders.
Our stock price is and may continue to be volatile
and you may not be able to resell our Common Stock at or above the price you paid.
The market price for our Common Stock is volatile
and may fluctuate significantly in response to a number of factors, many of which we cannot control, such as quarterly fluctuations in
financial results, the timing and our ability to advance the development of our product candidates or changes in securities analysts’
recommendations could cause the price of our stock to fluctuate substantially. In addition, stock markets generally have recently experienced
volatility. Our stock price is likely to experience significant volatility in the future. The price of our Common Stock may decline and
the value of any investment in our Common Stock may be reduced regardless of our performance. Further, the daily trading volume of our
Common Stock has historically been relatively low. As a result of the historically low volume, our shareholders may be unable to sell
significant quantities of Common Stock in the public trading markets without a significant reduction in the price of our shares of Common
Stock. Each of these factors, among others, could harm your investment in our Common Stock and could result in your being unable to resell
the shares of our Common Stock that you purchase at a price equal to or above the price you paid.
In the past, when the market price of a stock has
been volatile, holders of that stock have sometimes instituted securities class action litigation against the issuer. If any of our stockholders
were to bring such a lawsuit against us, we could incur substantial costs defending the lawsuit and the attention of our management would
be diverted from the operation of our business.
We do not intend to pay dividends on our Common
Stock, so any returns will be limited to the value of our Common Stock.
We currently anticipate that we will retain any future
earnings to finance the continued development, operation and expansion of our business. As a result, we do not anticipate declaring or
paying any cash dividends or other distributions in the foreseeable future. If we do not pay dividends, our Common Stock may be less valuable
because stockholders must rely on sales of their Common Stock after price appreciation, which may never occur, to realize any gains on
their investment.
You may experience
future dilution as a result of future equity offerings or if we issue shares subject to options, warrants, stock awards or other arrangements.
In order to raise additional
capital, we may in the future offer additional shares of our Common Stock or other securities convertible into or exchangeable for our
Common Stock, including under the ATM Agreement, pursuant to which the Company may issue and sell from time to time shares of Common Stock
through Cantor. We may sell shares or other securities in any other offering at a price per share that is less than the current market
price of our securities, and investors purchasing shares or other securities in the future could have rights superior to existing stockholders.
The sale of additional shares of Common Stock or other securities convertible into or exchangeable for our Common Stock would dilute all
of our stockholders, and if such sales of convertible securities into or exchangeable into our Common Stock occur at a deemed issuance
price that is lower than the current exercise price of our outstanding warrants sold to Acuitas Group Holdings, LLC (“Acuitas”)
in August 2022 (the “Acuitas Warrants”), the exercise price for those warrants would adjust downward to the deemed issuance
price pursuant to price adjustment protection contained within those warrants.
In addition, as of December
31, 2023, there were warrants outstanding to purchase an aggregate of 7,770,285 shares of Common Stock at exercise prices ranging
from $1.82 to $12.50 per share and 4,173,325 shares issuable upon exercise of outstanding options at exercise prices ranging from
$1.69 to $42.09 per share and restricted stock units totaling 687,428. Our Loan Agreement entered into on November 30, 2021 contains
a conversion feature whereby at the option of lender, up to $5 million of the outstanding loan amount may be converted into shares of
Common Stock at a conversion price of $6.98 per share. We may grant additional options, warrants or equity awards. To the extent such
shares are issued, the interest of holders of our Common Stock will be diluted.
Moreover, we are obligated
to issue shares of Common Stock upon achievement of certain clinical, regulatory and commercial milestones with respect to certain of
our drug candidates (i.e., NE3107, NE3291, NE3413, and NE3789) pursuant to the asset purchase agreement, dated April 27, 2021, by and
among the Company, NeurMedix, Inc. and Acuitas, as amended on May 9, 2021. The achievement of these milestones could result in the issuance
of up to 18 million shares of our Common Stock, further diluting the interest of holders of our Common Stock.
There is no established public trading market
for the Pre-funded Warrants or Common Warrants being offered in this offering, and we do not expect a market to develop for the Pre-funded
Warrants or Common Warrants.
There is no established public trading market for
the Pre-funded Warrants or Common Warrants being offered and sold in this offering, and we do not expect a market to develop. In addition,
we do not intend to apply to list the Pre-funded Warrants or Common Warrants on any national securities exchange or other nationally recognized
trading system. Without an active market, the liquidity of the Pre-funded Warrants or Common Warrants will be limited. Further, the existence
of the Pre-funded Warrants or Common Warrants may act to reduce both the trading volume and the trading price of our Common Stock.
The Pre-funded Warrants or Common Warrants are
speculative in nature.
Except as otherwise provided in the Pre-funded Warrants
or Common Warrants, until holders of Pre-funded Warrants or Common Warrants acquire our Common Stock upon exercise of the Pre-funded Warrants
or Common Warrants, holders of Pre-funded Warrants and Common Warrants will have no rights with respect to our Common Stock underlying
such Pre-funded Warrants and Common Warrants. Upon exercise of the Pre-funded Warrants or Common Warrants, the holders will be entitled
to exercise the rights of a stockholder of our Common Stock only as to matters for which the record date occurs after the exercise date.
Moreover, following this offering, the market value
of the Pre-funded Warrants and Common Warrants is uncertain. There can be no assurance that the market price of our Common Stock will
ever equal or exceed the price of the Pre-funded Warrants or Common Warrants, and, consequently, whether it will ever be profitable for
investors to exercise their Pre-funded Warrants or Common Warrants.
We will not receive any meaningful amount
of additional funds upon the exercise of the Pre-funded Warrants and Common Warrants.
Each Pre-funded Warrant and each Common
Warrant, respectively, will be exercisable until it is fully exercised
and by means of payment of the nominal cash purchase price upon exercise, or $1.50 cash purchase price upon exercise, respectively, or
through a “cashless exercise” procedure. Accordingly, we will not, in case of the Pre-funded Warrants, and may not, in case
of the Common Warrants, receive any meaningful additional funds upon the exercise of the Pre-funded Warrants or Common Warrants.
If we do not maintain a current and effective
prospectus relating to the Common Stock issuable upon exercise of the Pre-funded Warrants or the Common Warrants, holders will only be
able to exercise such Pre-funded Warrants or the Common Stock Purchase Warrants on a “cashless basis.”
If we do not maintain a current and effective prospectus
relating to the shares of Common Stock issuable upon exercise of the Pre-funded Warrants or the Common Warrants at the time that holders
wish to exercise such warrants, they will only be able to exercise them on a “cashless basis,” and under no circumstances
would we be required to make any cash payments or net cash settle such warrants to the holders. As a result, the number of shares of Common
Stock that holders will receive upon exercise of the Pre-funded Warrants or the Common Warrants will be fewer than it would have been
had such holders exercised their Pre-funded Warrants or the Common Warrants for cash. If we are unable to maintain a current and effective
prospectus, the potential “upside” of the holder’s investment in our company may be reduced.
Significant holders
or beneficial holders of shares of our Common Stock may not be permitted to exercise the Pre-funded Warrants that they hold.
A holder of the Pre-funded Warrants will not
be entitled to exercise any portion of any Pre-funded Warrant that, upon giving effect to such exercise, would cause: (i) the aggregate
number of shares of our Common Stock beneficially owned by such holder (together with its affiliates) to exceed 4.99% (or 9.99% at the
election of the holder) of the number of shares of our Common Stock immediately after giving effect to the exercise; or (ii) the combined
voting power of our securities beneficially owned by such holder (together with its affiliates) to exceed 4.99% (or 9.99% at the election
of the holder) of the combined voting power of all of our securities outstanding immediately after giving effect to the exercise, as such
percentage ownership is determined in accordance with the terms of the Pre-funded Warrants. As a result, you may not be able to exercise
your Pre-funded Warrants for shares of our Common Stock at a time when it would be financially beneficial for you to do so. In such
a circumstance, you could seek to sell your Pre-funded Warrants to realize value, but you may be unable to do so in the absence of
an established trading market and due to applicable transfer restrictions.
This is a best efforts offering, no minimum
number of securities is required to be sold, and we may not raise the amount of capital we believe is required for our business plans.
The placement agent has agreed to use its reasonable best efforts to solicit
offers to purchase the Shares, the Pre-funded Warrants, and the Common Warrants in this offering. The placement agent has no obligation
to buy any of the securities from us or to arrange for the purchase or sale of any specific number or dollar amount of the securities.
There is no required minimum number of securities or amount of proceeds that must be sold as a condition to completion of this offering.
Because there is no minimum number of securities or amount of proceeds required as a condition to the closing of this offering, the actual
offering amount, placement agent fees and proceeds to us are not presently determinable and may be substantially less than the maximum
amounts set forth above. We may sell fewer than all of the securities offered hereby, which may significantly reduce the amount of proceeds
received by us, and investors in this offering will not receive a refund in the event that we do not sell all of the units offered in
this offering. Thus, we may not raise the amount of capital we believe is required for our operations in the short term and may need to
raise additional funds, which may not be available or available on terms acceptable to us.
The Nasdaq Capital
Market may seek to delist our Common Stock if it concludes this offering does not qualify as a public offering as defined under Nasdaq’s
stockholder approval rule.
The continued listing of
our Common Stock on Nasdaq depends on our compliance with the requirements for continued listing under the Nasdaq Marketplace Rules, including,
but not limited to, Market Place Rule 5635, or the stockholder approval rule. The stockholder approval rule prohibits the issuance of
shares of Common Stock (or derivatives) in excess of 20% of our outstanding shares of Common Stock without stockholder approval, unless
those shares are sold at a price that equals or exceeds the “minimum price”, as defined in the stockholder approval rule,
or in what Nasdaq deems a “public offering” as defined in the stockholder approval rule (a “Public Offering”).
The securities sold in this offering may be sold at a significant discount to the “minimum price” as defined in the stockholder
approval rule, and we do not intend to obtain the approval of our stockholders for the issuance of the securities in this offering. Accordingly,
we have sought to conduct, and plan to continue to conduct, this offering as a Public Offering as defined in the stockholder approval
rule, which is a qualitative analysis based on several factors as determined by Nasdaq, including by broadly marketing and offering these
securities in a firm commitment underwritten offering registered under the Securities Act. Demand for the securities sold by us in this
offering, and the final offering price for these securities, will be determined following a broad public marketing effort over several
trading days, and final distribution of these securities will ultimately be determined by the placement agent. Nasdaq has also published
guidance that an offering of securities that are “deeply discounted” to the “minimum price” (for example a discount
of 50% or more) will typically preclude a determination that the offering qualifies as Public Offering for purposes of the stockholder
approval rule. We cannot assure you that Nasdaq will determine that this offering will be deemed a Public Offering under the stockholder
approval rule. If Nasdaq determines that this offering was not conducted in compliance with the stockholder approval rule, Nasdaq may
cite a deficiency and move to delist our securities from Nasdaq. Upon a delisting from Nasdaq, our stock would likely be traded in the
over-the-counter inter-dealer quotation system, more commonly known as the “OTC.” OTC transactions involve risks in addition
to those associated with transactions in securities traded on the securities exchanges, such as Nasdaq, or, together, Exchange-listed
stocks. Many OTC stocks trade less frequently and in smaller volumes than exchange-listed stocks. Accordingly, our stock would be less
liquid than it would be otherwise. Also, the prices of OTC stocks are often more volatile than Exchange-listed stocks. Additionally, institutional
investors are usually prohibited from investing in OTC stocks, and it might be more challenging to raise capital when needed.
We are currently subject to securities class
action litigation and may be subject to similar or other litigation in the future, all of which will require significant management time
and attention, result in significant legal expenses and may result in unfavorable outcomes, which may have a material adverse effect on
our business, operating results and financial condition, and negatively affect the price of our Common Stock.
We are, and may in the future become, subject to various
legal proceedings and claims that arise in or outside the ordinary course of business. For example, on January 19, 2024, a putative securities
class action, captioned Eric Olmstead v. BioVie Inc. et al., No. 3:24-cv-00035, was filed in the U.S. District Court for the District
of Nevada against the Company and certain of its officers and/or directors, seeking to recover damages for alleged violations of Sections
10(b) and 20(a) of the Securities Exchange Act of 1934, as amended (the "Exchange Act"). The complaint alleges that certain
statements the Company made between August 5, 2021 and November 29, 2023 about the Company’s business, operations and prospects,
including with respect to its Phase 3 study of NE3107 in Alzheimer’s Disease, were materially false and misleading in that they
omitted material adverse facts regarding that Phase 3 study, and that the plaintiff suffered losses when the Company’s stock price
dropped after it announced on November 29, 2023 that the Phase 3 study’s primary efficacy endpoint missed statistical significance
due to the unanticipated exclusion of all patient data from certain trial sites. The Company believes the claims are without merit and
intends to defend vigorously against them, but there can be no assurances as to the outcome.
It is possible that additional lawsuits will be filed,
or allegations received from stockholders or regulatory agencies, with respect to these same or other matters and also naming us and/or
our officers and directors as defendants. Such lawsuits and any other related proceedings are subject to inherent uncertainties, and the
actual defense and disposition costs will depend upon many unknown factors. The outcomes of such matters are necessarily uncertain. We
could be forced to expend significant resources in the defense of the pending lawsuit and any additional proceedings, and we may not prevail.
In addition, we may incur substantial legal fees and costs in connection with such matters. Furthermore, our articles of incorporation
and bylaws require us to indemnify our officers and directors against claims associated with carrying out the duties of their offices.
We are also required to advance the costs of certain legal defenses upon the indemnitee undertaking to repay such expenses to the extent
it is later determined that such person was not entitled to indemnification of such expenses. Thus we currently are not able to estimate
the possible cost to us from the pending lawsuit as it is currently at an early stage, and we cannot be certain how long it may take to
resolve the lawsuit or the possible damages that we may be required to pay. Monitoring, initiating and defending against legal actions
is time-consuming for our management, is likely to be expensive and may detract from our ability to fully focus our internal resources
on our business activities. We could be forced to expend significant resources in the defense and settlement of the pending lawsuit and
any potential future lawsuits or proceedings, and we may not prevail in such matters.
We have insurance coverage that we believe applies
to the pending lawsuit and potentially to related matters. That said, the extent to which our insurance will offset liabilities arising
from pending lawsuit and potentially to related matters is uncertain. Among other things, our insurance does not apply until we have satisfied
an out-of-pocket retention, it may be determined that our insurance coverage does not cover the pending lawsuit or related matters (in
whole or in part), or the amount of our insurance limits may not be sufficient to cover our liabilities arising from the pending lawsuit
and related matters. In addition, we may have rights of recovery against certain third parties, including CROs and clinical testing sites,
with respect to the allegations and damages sought in the pending lawsuit. Although such rights may, in addition to insurance, help offset
our losses from the pending lawsuit, whether and to what extent we are able to secure proceeds from insurance and other third parties
is uncertain at this time.
A decision adverse to our interests in the pending
lawsuit, or in related matters, could result in our being liable for payment of substantial damages, or possibly fines, and could have
a material adverse effect on our business, our stock price, cash flow, results of operations and financial condition. The extent of such
effect may depend, at least in part, on our ability to offset our losses by proceeds from third parties, including our insurers and other
third-party indemnitors. As discussed above, however, whether and to what extent we are able to secure proceeds from these parties currently
is uncertain. At this time, we have not established any reserves for any potential liability relating to the pending lawsuit or any potential
future lawsuits. Any judgments, settlements, or fines in current or future litigation could have a material adverse effect on our business,
operating results or financial condition. In addition, such lawsuits or related matters may make it more difficult for us to finance our
operations and adversely affect our ability to make payments for such judgments, settlements, or fines.
Risks Relating to Our Intellectual Property
We may be unable to obtain or protect intellectual
property rights relating to our product candidates, which could have a materially adverse effect on our business.
Our ability to compete effectively
will depend on our ability to maintain the proprietary nature of our technologies. We cannot assure investors that we will continue to
innovate and file new patent applications, or that if filed any future patent applications will result in granted patents with respect
to the technology owned by us or licensed to us. Further, we cannot predict how long it will take for such patents to issue, if at all.
The patent position of pharmaceutical or biotechnology companies, including ours, is generally uncertain and involves complex legal and
factual considerations and, therefore, validity and enforceability cannot be predicted with certainty. Patents may be challenged, deemed
unenforceable, invalidated or circumvented.
The Company has also filed a Patent Cooperation Treaty (“PCT”) application
covering our novel liquid formulations of terlipressin (international patent application PCT/US2020/034269 published as WO2020/237170),
and we are seeking patent protection in the United States, Europe, China, Japan and at eight other jurisdictions. We also have 14 issued
U.S. patents, seven (7) pending U.S. applications, three (3) pending PCT applications, six (6) issued foreign patents, and six (6) pending
foreign patent applications directed to protecting NE3107 and related compounds and methods of making and using thereof. However, there
can be no assurance that our pending patent applications will result in issued patents, or that any issued patent claims from pending
or future patent applications will be sufficiently broad to protect BIV201, NE3107, or any other product candidates or to provide us with
competitive advantages.
We
can provide no assurance that any issued patents will provide us with any competitive
advantage. We cannot be certain that there is no invalidating prior art of which we and the patent examiner are unaware or that our interpretation
of the relevance of prior art is correct. If a third-party patent or patent application is determined to have an earlier priority date,
it may prevent our patent applications from issuing at all or issuing in a form that provides any competitive advantage for our drug candidates.
Failure to obtain additional issued patents could have a material adverse effect on our ability to develop and commercialize our drug
candidates. Even if our patent applications do issue as patents, third parties may be able to challenge the validity and enforceability
of our patents on a variety of grounds, including that such third party’s patents and patent applications have an earlier priority
date, and if such challenges are successful, we may be required to obtain one or more licenses from such third parties, if available on
commercially reasonable terms, or be prohibited from commercializing our drug candidates.
We
seek to protect our proprietary positions by, among other things, filing patent
applications in the United States and abroad related to our current drug candidates and other drug candidates that we may identify. Obtaining,
maintaining, defending and enforcing pharmaceutical patents is costly, time-consuming and complex, and we may not be able to file and
prosecute all necessary or desirable patent applications, or maintain, enforce and license any patents that may issue from such patent
applications, at a reasonable cost or in a timely manner. It is also possible that we will fail to identify patentable aspects of our
research and development output before it is too late to obtain patent protection. Moreover, under certain of our license or collaboration
agreements, we may not have the right to control the preparation, filing, prosecution and maintenance of patent applications, or to maintain
the rights to patents licensed to or from third parties.
We
currently are the assignee of a number of U.S. provisional patent applications. U.S. provisional patent applications are not eligible
to become issued patents until, among other things, we file a non-provisional patent application within 12 months of filing one or more
of our related provisional patent applications. With regard to such U.S. provisional patent applications, if we do not timely file any
non-provisional patent applications, we may lose our priority dates with respect to our provisional patent applications and any patent
protection on the inventions disclosed in our provisional patent applications. Further, in the event that we do timely file non-provisional
patent applications relating to our provisional patent applications, we cannot predict whether any such patent applications will result
in the issuance of patents or if such issued patents will provide us with any competitive advantage.
Although
we enter into confidentiality agreements with parties who have access to confidential or patentable aspects of our research and development
output, such as our employees, collaborators, CROs, contract manufacturers, consultants, advisors and other third parties, any of these
parties may breach these agreements and disclose such output before a patent application is filed, thereby jeopardizing our ability to
seek patent protection. Further, we may not be aware of all third-party intellectual property rights potentially relating to our drug
candidates. Publications of discoveries in the scientific literature often lag behind the actual discoveries, and patent applications
in the United States and other jurisdictions are typically not published until 18 months after filing or, in some cases, not at all. Therefore,
we cannot know with certainty whether we were the first to make the inventions claimed in our patents or pending patent applications,
or that we were the first to file for patent protection of such inventions.
The
patent position of pharmaceutical companies generally is highly uncertain, involves complex legal, technological and factual questions
and has, in recent years, been the subject of much debate and litigation throughout the world. In addition, the laws of foreign countries
may not protect our rights to the same extent as the laws of the United States, or vice versa. The standards that the United States Patent
and Trademark Office (the “USPTO”) (and foreign countries) use to grant patents are not always applied predictably or uniformly
and can change. There is also no uniform, worldwide policy regarding the subject matter and scope of claims granted or allowable in pharmaceutical
or biotechnology patents. Accordingly, we do not know the degree of future protection for our proprietary rights or the breadth of claims
that will be allowed in any patents issued to us or to others. The issuance, scope, validity, enforceability, and commercial value of
our patent rights are highly uncertain. The subject matter claimed in a patent application can be significantly reduced or eliminated
before the patent issues, if at all, and its scope can be reinterpreted or narrowed after issuance. Therefore, our pending and future
patent applications may not result in patents being issued in relevant jurisdictions that protect our drug candidates, in whole or in
part, or that effectively prevent others from commercializing competitive drug candidates, and even if our patent applications issue as
patents in relevant jurisdictions, they may not issue in a form that will provide us with any meaningful protection for our drug candidates
or technology, prevent competitors from competing with us or otherwise provide us with any competitive advantage. Additionally, our competitors
may be able to circumvent our patents by challenging their validity or by developing similar or alternative drug candidates or technologies
in a non-infringing manner.
The
issuance of a patent is not conclusive as to its inventorship, scope, validity or enforceability, and our patents may be challenged in
the courts or patent offices in the United States and abroad. We may be subject to a third-party preissuance submission of prior art to
the USPTO, or become involved in opposition, derivation, reexamination, inter partes review, post-grant review or interference
proceedings challenging our patent rights or the patent rights of others, or other proceedings in the USPTO or applicable foreign offices
that challenge priority of invention or other features of patentability. An adverse determination in any such submission, proceeding or
litigation could result in loss of exclusivity or ability to sell our products free from infringing the patents of third parties, patent
claims being narrowed, invalidated or held unenforceable, in whole or in part, and limitation of the scope or duration of the patents
directed to our drug candidates, all of which could limit our ability to stop others from using or commercializing similar or identical
drug candidates or technology to compete directly with us, without payment to us, or result in our inability to manufacture or commercialize
drug candidates or approved products (if any) without infringing third-party patent rights. In addition, if the breadth or strength of
the claims of our patents and patent applications is threatened, regardless of the outcome, it could dissuade companies from collaborating
with us to license, develop or commercialize current or future drug candidates, or could have a material adverse effect on our ability
to raise funds necessary to continue our research programs or clinical trials. Such proceedings also may result in substantial cost and
require significant time from our scientists and management, even if the eventual outcome is favorable to us.
In
addition, given the amount of time required for the development, testing and regulatory review of new drug candidates, patents protecting
such candidates might expire before or shortly after such candidates are commercialized. As a result, our patent portfolio may not provide
us with sufficient rights to exclude others from commercializing products or technology similar or identical to ours for a meaningful
amount of time, or at all. Moreover, some of our licensed patents and owned or licensed patent applications may in the future be co-owned
with third parties. If we are unable to obtain exclusive licenses to any such co-owners’ interest in such patents or patent applications,
such co-owners may be able to license their rights to other third parties, including our competitors, and our competitors could market
competing products and technology. In addition, we may need the cooperation of any such co-owners in order to enforce such patents against
third parties, and such cooperation may not be provided to us. Any of the foregoing could harm our competitive position, business, financial
condition, results of operations and prospects.
Further,
we rely on a combination of trade secrets, know-how, technology and nondisclosure, and other contractual agreements and technical measures
to protect our rights in the technology. If any trade secret, know-how or other technology not protected by a patent were to be disclosed
to or independently developed by a competitor, our business and financial condition could be materially and adversely affected. The laws
of some foreign countries do not protect our proprietary rights to the same extent as the laws of the U.S., and we may encounter significant
problems in protecting our proprietary rights in these countries.
Our success
depends in significant part on our ability to obtain, maintain, enforce and defend patents and other intellectual property rights with
respect to our drug candidates and technology and to operate our business without infringing, misappropriating, or otherwise violating
the intellectual property rights of others. If we are unable to obtain and maintain sufficient intellectual property protection for our
drug candidates or other drug candidates that we may identify, or if the scope of the intellectual property protection obtained is not
sufficiently broad, our competitors and other third parties could develop and commercialize drug candidates similar or identical to ours,
and our ability to successfully commercialize our drug candidates and other drug candidates that we may pursue may be impaired.
Confidentiality agreements with employees and
others may not adequately prevent disclosure of trade secrets and other proprietary information and disclosure of our trade secrets or
proprietary information could compromise any competitive advantage that we have, which could have a materially adverse effect on our business.
Our success depends, in part,
on our ability to protect our proprietary rights to the technologies used in our product candidates. We depend heavily upon confidentiality
agreements with our officers, employees, consultants and subcontractors to maintain the proprietary nature of our technology. These measures
may not afford us complete or even sufficient protection, and may not afford an adequate remedy in the event of an unauthorized disclosure
of confidential information. If we fail to protect and/or maintain our intellectual property, third parties may be able to compete more
effectively against us, we may lose our technological or competitive advantage, and/or we may incur substantial litigation costs in our
attempts to recover or restrict use of our intellectual property. In addition, others may independently develop technology similar to
ours, otherwise avoiding the confidentiality agreements, or produce patents that would materially and adversely affect our business, prospects,
financial condition and results of operations, in which event you could lose all of your investment.
We may enter into licensing
and collaboration agreements with third parties. If we fail to comply with our obligations in the agreements under which we license intellectual
property rights to or from third parties, or these agreements are terminated, or we otherwise experience disruptions to our business relationships
with our licensors or licensees, our competitive position, business, financial condition, results of operations and prospects could be
harmed.
It
may be necessary for us to use the patented or proprietary technology of third parties to commercialize our products (if approved), in
which case we would be required to obtain a license from these third parties. The licensing of third-party intellectual property rights
is a competitive area, and more established companies may pursue strategies to license or acquire third-party intellectual property rights
that we may consider attractive or necessary. More established companies may have a competitive advantage over us due to their size, capital
resources and greater clinical development and commercialization capabilities. In addition, companies that perceive us to be a competitor
may be unwilling to assign or license rights to us. We also may be unable to license or acquire third-party intellectual property rights
on terms that would allow us to make an appropriate return on our investment or at all. If we are unable to license such technology, or
if we are forced to license such technology on unfavorable terms, our business could be materially harmed.
We
may fail to obtain any of these licenses or intellectual property rights on commercially reasonable terms. Even if we are able to obtain
a license, it may be non-exclusive, thereby giving our competitors access to the same technologies licensed to us. Licenses may not provide
us with exclusive rights to use the applicable intellectual property and technology in all relevant fields of use and in all territories
in which we may wish to develop or commercialize our drug candidates, products (if approved) and technology in the future. In that event,
we may be required to expend significant time and resources to develop or license replacement technology. If we are unable to do so, we
may be unable to develop or commercialize the affected products, which could materially harm our business and the third parties owning
such intellectual property rights could seek either an injunction prohibiting our sales, or, with respect to our sales, an obligation
on our part to pay royalties and/or other forms of compensation. Conversely, we may not always be able to successfully pursue our claims
against others that infringe upon our technology. Thus, the proprietary nature of our technology or technology licensed by us may not
provide adequate protection against competitors, and we may not be able to prevent competitors from developing and commercializing competitive
products or technologies.
In
addition, in some circumstances, we may not have the right to control the preparation, filing and prosecution of patent applications or
to maintain, defend and enforce the patents that we license to or from third parties, and we may have to rely on our partners to fulfill
these responsibilities. If our current or future licensors, licensees or collaborators fail to prepare, file, prosecute, maintain, enforce,
and defend licensed patents and other intellectual property rights, such rights may be reduced or eliminated, and our right to develop
and commercialize any of our drug candidates or technology that are the subject of such licensed rights could be adversely affected. In
addition, our licensors may own or control intellectual property that has not been licensed to us and, as a result, we may be subject
to claims, regardless of their merit, that we are infringing or otherwise violating the licensor’s rights.
If we fail to comply with
our obligations, including the obligation to make various milestone payments and royalty payments, under any of the agreements under
which we license intellectual property rights from third parties, the licensor may have the right to terminate the license. If any
of our license agreements is terminated, the underlying licensed patents fail to provide the intended exclusivity or we otherwise
experience disruptions to our business relationships with our licensors, we could lose intellectual property rights that are
important to our business or be prevented from developing and commercializing our drug candidates, and competitors could have the
freedom to seek regulatory approval of, and to market, products identical to ours. Termination of these agreements or reduction or
elimination of our rights under these agreements may also result in our having to negotiate new or reinstated agreements with less
favorable terms, cause us to lose our rights under these agreements, including our rights to important intellectual property or
technology, or impede, delay or prohibit the further development or commercialization of one or more drug candidates that rely on
such agreements. It is possible that we may be unable to obtain any additional licenses at a reasonable cost or on reasonable terms,
if at all. In that event, we may be required to expend significant time and resources to redesign our drug candidates or the methods
for manufacturing them or to develop or license replacement technology, all of which may not be feasible on a technical or
commercial basis.
Licensing
of intellectual property is of critical importance to our business and involves complex legal, business and scientific issues and certain
provisions in intellectual property license agreements may be susceptible to multiple interpretations. Disputes may arise between us and
our licensing partners regarding intellectual property subject to a license agreement, including:
| · | the scope of rights granted under the license agreement and other interpretation-related issues; |
| · | whether and the extent to which technology and processes of one party infringe intellectual property of the other party that are not
subject to the licensing agreement; |
| · | rights to sublicense patent and other rights to third parties; |
| · | any diligence obligations with respect to the use of the licensed technology in relation to development and commercialization of our
drug candidates, and what activities satisfy those diligence obligations; |
| · | the ownership of inventions and know-how resulting from the joint creation or use of intellectual property; |
| · | rights to transfer or assign the license; and |
| · | the effects of termination. |
The
resolution of any contract interpretation disagreement that may arise could narrow what we believe to be the scope of our rights to the
relevant intellectual property or technology, or increase what we believe to be our financial or other obligations under the relevant
agreement, either of which could harm our business, financial condition, results of operations and prospects. If disputes over intellectual
property that we have licensed prevent or impair our ability to maintain our current licensing arrangements on acceptable terms or at
all, we may be unable to successfully develop and commercialize the affected drug candidates. Moreover, any dispute or disagreement with
our licensing partners may result in the delay or termination of the research, development or commercialization of our drug candidates
or any future drug candidates, and may result in costly litigation or arbitration that diverts management attention and resources away
from our day-to-day activities, which may adversely affect our business, financial condition, results of operations and prospects.
Furthermore,
current and future collaborators or strategic partners may develop, either alone or with others, products in related fields that are competitive
with the products or potential products that are the subject of these collaborations. Competing products, either developed by our collaborators
or strategic partners or to which the collaborators or strategic partners have rights, may result in the withdrawal of partner support
for our drug candidates. Any of these developments could harm our product development efforts.
In
addition, if our licensors fail to abide by the terms of the license, if the licensors fail to prevent infringement by third parties or
if the licensed patents or other rights are found to be invalid or unenforceable, our business, competitive position, financial condition,
results of operations and prospects could be materially harmed.
Some of our intellectual
property may be subject to federal regulations such as “march-in” rights, certain reporting requirements and a preference
for U.S.-based companies if it is determined that our intellectual property has been discovered through government-funded programs. Compliance
with such regulations may limit our exclusive rights, and limit our ability to contract with non-U.S. manufacturers.
Some
of the intellectual property rights we have acquired or licensed or may acquire or license in the future may have been generated through
the use of U.S. government funding and may therefore be subject to certain federal regulations. These U.S. government rights include a
non-exclusive, non-transferable, irrevocable worldwide license to use inventions for any governmental purpose. In addition, the U.S. government
has the right, under certain limited circumstances, to require us to grant exclusive, partially exclusive, or non-exclusive licenses to
any of these inventions to a third party if it determines that: (i) adequate steps have not been taken to commercialize the invention;
(ii) government action is necessary to meet public health or safety needs; or (iii) government action is necessary to meet requirements
for public use under federal regulations (also referred to as “march-in rights”). The U.S. government also has the right to
take title to these inventions if the grant recipient fails to disclose the invention to the government or fails to file an application
to register the intellectual property within specified time limits. Intellectual property generated under a government funded program
is also subject to certain reporting requirements, compliance with which may require us to expend substantial resources. In addition,
the U.S. government requires that any products embodying any of these inventions or produced through the use of any of these inventions
be manufactured substantially in the United States. This preference for U.S. industry may be waived by the federal agency that provided
the funding if the owner or assignee of the intellectual property can show that reasonable but unsuccessful efforts have been made to
grant licenses on similar terms to potential licensees that would be likely to manufacture substantially in the United States or that
under the circumstances domestic manufacture is not commercially feasible. This preference for U.S. industry may limit our ability to
contract with non-U.S. product manufacturers for products relating to such intellectual property. To the extent any of our future intellectual
property is also generated through the use of U.S. government funding, the provisions of the Bayh-Dole Act may similarly apply.
Patent terms may be
inadequate to establish our competitive position on our drug candidates for an adequate amount of time.
Patents
have a limited lifespan. In the United States, if all maintenance fees are timely
paid, the natural expiration of a patent is generally 20 years from its earliest U.S. non-provisional filing date. Various extensions
may be available, but the life of a patent, and the protection it affords, is limited. Even if patents directed to our drug candidates
are obtained, once the patent life has expired for a drug candidate, we may be open to competition from competitive medications, including
generic versions. Given the amount of time required for the development, testing and regulatory review of new drug candidates, patents
directed towards such drug candidates might expire before or shortly after such drug candidates are commercialized. As a result, our owned
and licensed patent portfolio may not provide us with sufficient rights to exclude others from commercializing drug candidates similar
or identical to ours for a meaningful amount of time, or at all.
Depending
upon the timing, duration and conditions of any FDA marketing approval of our drug candidates, one or more of our owned or licensed U.S.
patents may be eligible for limited patent term extension under the Hatch-Waxman Act, and similar legislation in the European Unition
(the “EU”) and certain other countries. The Hatch-Waxman Act permits a patent term extension of up to five years for a patent
covering an approved product as compensation for effective patent term lost during product development and the FDA regulatory review process.
However, we may not receive an extension if we fail to exercise due diligence during the testing phase or regulatory review process, fail
to apply within applicable deadlines, fail to apply prior to expiration of relevant patents or otherwise fail to satisfy applicable requirements.
Moreover, the length of the extension could be less than we request. Only one patent per approved product can be extended, the extension
cannot extend the total patent term beyond 14 years from approval and only those claims for the approved drug, a method for using it or
a method for manufacturing it may be extended. If we are unable to obtain patent term extension or the term of any such extension is less
than we request, the period during which we can enforce our patent rights for the applicable drug candidate will be shortened and our
competitors may obtain approval to market competing products sooner. As a result, our revenue from applicable products could be reduced.
Further, if this occurs, our competitors may take advantage of our investment in development and trials by referencing our clinical and
nonclinical data and launch their product earlier than might otherwise be the case, and our competitive position, business, financial
condition, results of operations and prospects could be materially harmed.
We may not be able
to protect our intellectual property rights throughout the world.
Filing,
prosecuting, maintaining, defending and enforcing patents on our drug candidates in all countries throughout the world would be prohibitively
expensive, and consequently our intellectual property rights in some countries outside the United States may be less extensive than those
in the United States. In addition, the laws of some foreign countries do not protect intellectual property rights to the same extent as
federal and state laws in the United States. Consequently, we may not be able to prevent third parties from practicing our inventions
in all countries outside the United States, or from selling or importing products made using our inventions in and into the United States
or other jurisdictions. Competitors may use our technologies in jurisdictions where we have not obtained patents to develop their own
products and may export otherwise infringing products to territories where we have patents, but enforcement rights are not as strong as
those in the United States. These products may compete with our drug candidates and our patents or other intellectual property rights
may not be effective or sufficient to prevent them from competing.
Many
companies have encountered significant problems in protecting and defending intellectual property rights in foreign jurisdictions. The
legal systems of some countries do not favor the enforcement or protection of patents, trade secrets and other intellectual property,
which could make it difficult for us to stop the infringement of our patents or marketing of competing products in violation of our intellectual
property and proprietary rights generally. Proceedings to enforce our intellectual property rights in foreign jurisdictions could result
in substantial costs and divert our efforts and attention from other aspects of our business, could put our patents at risk of being invalidated
or interpreted narrowly and our patent applications at risk of not issuing and could provoke third parties to assert claims against us.
We may not prevail in any lawsuits that we initiate, and the damages or other remedies awarded, if any, may not be commercially meaningful.
Many
foreign countries, including some EU countries, India, Japan and China, have compulsory licensing laws under which a patent owner may
be compelled under specified circumstances to grant licenses to third parties. In addition, many countries limit the enforceability of
patents against government agencies or government contractors. In those countries, we may have limited remedies if patents are infringed
or if we are compelled to grant a license to a third party, which could materially diminish the value of the applicable patents and limit
our potential revenue opportunities. Accordingly, our efforts to enforce our intellectual property rights around the world may be inadequate
to obtain a significant commercial advantage from the intellectual property that we develop or license, which could adversely affect our
business, financial condition, results of operations and prospects.
In
2012, the European Patent Package, or EU Patent Package, regulations were passed with the goal of providing a single pan-European Unitary
Patent and a new European Unified Patent Court (“UPC”), for litigation involving European patents. Implementation of the EU
Patent Package occurred in 2023. Under the UPC, all European patents, including those issued prior to ratification of the European Patent
Package, will by default automatically fall under the jurisdiction of the UPC. The UPC will provide our competitors with a new forum to
centrally revoke our European patents, and allow for the possibility of a competitor to obtain pan-European injunctions. It will be several
years before we will understand the scope of patent rights that will be recognized and the strength of patent remedies that will be provided
by the UPC. Under the EU Patent Package as currently proposed, we will have the right to opt our patents out of the UPC over the first
seven years of the court’s existence, but doing so may preclude us from realizing the benefits of the new unified court.
Changes in patent law
could diminish the value of patents in general, thereby impairing our ability to protect our drug candidates.
Obtaining
and enforcing patents in the pharmaceutical industry is inherently uncertain, due in part to ongoing changes in the patent laws. For example,
in the United States, depending on decisions by Congress, the federal courts, and the USPTO, the laws and regulations governing patents,
and interpretation thereof, could change in unpredictable ways that could weaken our and our collaborators’ or licensors’
ability to obtain new patents or to enforce existing or future patents. For example, the U.S. Supreme Court has ruled on several patent
cases in recent years, either narrowing the scope of patent protection available in certain circumstances or weakening the rights of patent
owners in certain situations. Therefore, there is increased uncertainty with regard to our and our collaborators’ or licensors’
ability to obtain patents in the future, as well as uncertainty with respect to the value of patents once obtained.
Patent
reform legislation could increase the uncertainties and costs surrounding the prosecution
of our and our collaborators’ or licensors’ patent applications and the enforcement or defense of our or our collaborators’
or licensors’ issued patents. For example, assuming that other requirements for patentability are met, prior to March 2013, in the
United States, the first to invent the claimed invention was entitled to the patent, while outside the United States, the first to file
a patent application was entitled to the patent. After March 2013, under the Leahy-Smith America Invents Act (the “Leahy-Smith Act”),
enacted in September 2011, the United States transitioned to a first inventor to file system in which, assuming that other requirements
for patentability are met, the first inventor to file a patent application will be entitled to the patent on an invention regardless of
whether a third party was the first to invent the claimed invention. The Leahy-Smith Act also includes a number of significant changes
that affect the way patent applications are prosecuted and may also affect patent litigation. These include allowing third-party submission
of prior art to the USPTO during patent prosecution and additional procedures to challenge the validity of a patent by USPTO-administered
post-grant proceedings, including post-grant review, inter partes review and derivation proceedings. The USPTO has developed regulations
and procedures to govern administration of the Leahy-Smith Act, and many of the substantive changes to patent law associated with the
Leahy-Smith Act, particularly the first inventor-to-file provisions. Accordingly, it is not clear what, if any, impact the Leahy-Smith
Act will have on the operation of our business. However, the Leahy-Smith Act and its implementation could increase the uncertainties and
costs surrounding the prosecution of our or our licensors’ patent applications and the enforcement or defense of our or our licensors’
issued patents. Similarly, statutory or judicial changes to the patent laws of other countries may increase the uncertainties and costs
surrounding the prosecution of patent applications and the enforcement or defense of issued patents. Any of the foregoing could harm our
business, financial condition, results of operations and prospects.
We may become involved
in lawsuits to protect or enforce our patents or other intellectual property, which could be expensive, time-consuming and unsuccessful,
and issued patents directed towards our technology and drug candidates could be found invalid or unenforceable if challenged.
We
are not aware that our patents directed to either BIV201 or NE3107, the product candidates we are currently developing, are infringed
by third parties. However, there can be no assurance that our patents will not be found in the future to be infringed by others. Any patents
we do obtain may be challenged by reexamination or otherwise invalidated or eventually found unenforceable. Both the patent application
process and the process of managing patent disputes can be time-consuming and expensive.
Significantly,
our pending patent applications cannot be enforced against third parties practicing the technology claimed in such applications unless
and until a patent issues from such applications. Our ability to enforce patent rights also depends on our ability to identify infringement.
It may be difficult to identify infringers who do not advertise the components or methods that are used in connection with their products
and services. Moreover, it may be difficult or impossible to obtain evidence of infringement in a competitor’s or potential competitor’s
product or service. Any claims we assert against perceived infringers could provoke these parties to assert counterclaims against us alleging
that we infringe their patents or that our patents are invalid or unenforceable. In a patent infringement proceeding, a court may decide
that a patent of ours is invalid or unenforceable, in whole or in part, construe the patent’s claims narrowly or refuse to stop
the other party from using the technology at issue on the grounds that our patents do not cover the technology. An adverse result in any
litigation proceeding could put one or more of our owned or licensed patents at risk of being invalidated, held unenforceable or interpreted
narrowly. We may find it impractical or undesirable to enforce our intellectual property against some third parties.
If we were to initiate legal proceedings against a third party to enforce a patent directed
to our drug candidates, or one of our future drug candidates, the defendant could counterclaim that our patent is invalid or unenforceable.
In patent litigation in the United States, defendant counterclaims alleging invalidity or unenforceability are commonplace. Grounds for
a validity challenge could be an alleged failure to meet any of several statutory requirements, including lack of novelty, obviousness,
non-enablement or insufficient written description. Grounds for a presentability assertion could be an allegation that someone connected
with prosecution of the patent withheld material information from the USPTO or made a misleading statement during prosecution. Third parties
may also raise similar claims before the USPTO or an equivalent foreign body, even outside the context of litigation. Potential proceedings
include reexamination, post-grant review, inter partes review, interference proceedings, derivation proceedings and equivalent
proceedings in foreign jurisdictions (e.g., opposition proceedings). Such proceedings could result in the revocation of, cancellation
of, or amendment to our patents in such a way that they no longer cover our technology or any drug candidates that we may develop. The
outcome following legal assertions of invalidity and unenforceability is unpredictable. With respect to the validity question, for example,
we cannot be certain that there is no invalidating prior art of which we and the patent examiner were unaware during prosecution. These
assertions may also be based on information known to us or the USPTO. If a defendant were to prevail on a legal assertion of invalidity
or unenforceability, we would lose at least part, and perhaps all, of the patent rights directed towards the applicable drug candidates
or technology related to the patent rendered invalid or unenforceable. Such a loss of patent rights would materially harm our business,
financial condition, results of operations and prospects.
Interference
proceedings provoked by third parties or brought by us or declared by the USPTO may be necessary to determine the priority of inventions
with respect to our patents or patent applications. An unfavorable outcome could require us to cease using the related technology or to
attempt to license rights to it from the prevailing party. Our business could be materially harmed if the prevailing party does not offer
us a license on commercially reasonable terms or at all.
Furthermore,
because of the substantial amount of discovery required in connection with intellectual property litigation, there is a risk that some
of our confidential information could be compromised by disclosure during this type of litigation.
The
pharmaceutical industry is characterized by extensive litigation regarding patents and other intellectual property rights. Moreover, the
cost to us of any litigation or other proceeding relating to our patents and other intellectual property rights, even if resolved in our
favor, could be substantial, and the litigation would divert our management’s efforts. We may not have sufficient resources to bring
any such action to a successful conclusion. Uncertainties resulting from the initiation and continuation of any litigation could limit
our ability to continue our operations and you could lose all of your investment.
Some
of our competitors are larger than we are and have substantially greater
resources. They are, therefore, likely to be able to sustain the costs of complex patent litigation or proceedings more effectively than
we can because of their greater financial resources and more mature and developed intellectual property portfolios. Accordingly, despite
our efforts, we may not be able to prevent third parties from infringing, misappropriating or otherwise violating our intellectual property.
Even if resolved in our favor, litigation or other legal proceedings relating to intellectual property claims could result in substantial
costs and diversion of management resources, which could harm our business. In addition, the uncertainties associated with litigation
could compromise our ability to raise the funds necessary to continue our clinical trials, continue our internal research programs, or
in-license needed technology or other drug candidates. There could also be public announcements of the results of the hearing, motions,
or other interim proceedings or developments. If securities analysts or investors perceive those results to be negative, it could cause
the price of shares of our Common Stock to decline. Any of the foregoing events could harm our business, financial condition, results
of operation and prospects.
We may not identify
relevant third-party patents or may incorrectly interpret the relevance, scope or expiration of a third-party patent, which might subject
us to infringement claims or adversely affect our ability to develop and market our drug candidates.
We
cannot guarantee that any of our or our licensors’ patent searches or analyses, including the identification of relevant patents,
the scope of patent claims or the expiration of relevant patents, are complete or thorough, nor can we be certain that we have identified
each and every third-party patent and pending patent application in the United States and abroad that is relevant to or necessary for
the commercialization of our drug candidates in any jurisdiction. For example, U.S. patent applications filed before November 29, 2000
and certain U.S. patent applications filed after that date that will not be filed outside the United States remain confidential until
patents issue. As mentioned above, patent applications in the United States and elsewhere are published approximately 18 months after
the earliest filing for which priority is claimed, with such earliest filing date being commonly referred to as the priority date. Therefore,
patent applications covering our drug candidates could have been filed by third parties without our knowledge. Additionally, pending patent
applications that have been published can, subject to certain limitations, be later amended in a manner that could cover our drug candidates
or the use of our drug candidates. The scope of a patent claim is determined by an interpretation of the law, the written disclosure in
a patent and the patent’s prosecution history. Our interpretation of the relevance or the scope of a patent or a pending application
may be incorrect, which may negatively impact our ability to market our drug candidates. We may incorrectly determine that our drug candidates
are not covered by a third-party patent or may incorrectly predict whether a third party’s pending application will issue with claims
of relevant scope. Our determination of the expiration date of any patent in the United States or abroad that we consider relevant may
be incorrect, which may negatively impact our ability to develop and market our drug candidates. Our failure to identify and correctly
interpret relevant patents may negatively impact our ability to develop and market our drug candidates.
In
addition, if we fail to identify and correctly interpret relevant patents, we may be subject to infringement claims. We cannot guarantee
that we will be able to successfully settle or otherwise resolve such infringement claims. If we fail in any such dispute, in addition
to being forced to pay damages, which may be significant, we may be temporarily or permanently prohibited from commercializing any of
our drug candidates that are held to be infringing. We might, if possible, also be forced to redesign drug candidates so that they no
longer infringe the third-party intellectual property rights. Any of these events, even if we were ultimately to prevail, could require
us to divert substantial financial and management resources that we would otherwise be able to devote to our business and could adversely
affect our business, financial condition, results of operations and prospects.
Third parties may initiate
legal proceedings alleging that we are infringing, misappropriating or otherwise violating their intellectual property rights, the outcome
of which would be uncertain and could negatively impact the success of our business.
Our
commercial success depends upon our ability to develop, manufacture, market and sell
our drug candidates and use our proprietary technologies without infringing, misappropriating or otherwise violating the intellectual
property and other proprietary rights of third parties. There is considerable intellectual property litigation in the pharmaceutical industry.
We may become party to, or be threatened with, future adversarial proceedings or litigation regarding intellectual property rights with
respect to our drug candidates and their manufacture and our other technology, including reexamination, interference, post-grant review,
inter partes review or derivation proceedings before the USPTO or an equivalent foreign body. Numerous U.S.- and foreign-issued
patents and pending patent applications owned by third parties exist in the fields in which we are developing our drug candidates. Third
parties may assert infringement claims against us based on existing patents or patents that may be granted in the future, regardless of
their merit.
We
do not believe that either BIV201 or NE3107, the product candidates we are currently developing, infringe the patents of any third parties.
However, there can be no assurance that our technology will not be found in the future to infringe the patents of others. Moreover, patent
applications are in some cases maintained in secrecy until patents are issued. The publication of discoveries in the scientific or patent
literature frequently occurs substantially later than the date on which the underlying discoveries were made and patent applications were
filed. Because patents can take many years to issue, there may be currently pending applications of which we are unaware that may later
result in issued patents that our products or product candidates infringe. For example, pending applications may exist that provide support
or can be amended to provide support for a claim that results in an issued patent that our product infringes.
Even
if we believe third-party intellectual property claims are without merit, there is no assurance that a court would find in our favor on
questions of claim scope, infringement, validity, enforceability or priority. A court of competent jurisdiction could hold that third-party
patents asserted against us are valid, enforceable and infringed, which could materially and adversely affect our ability to commercialize
any drug candidates we may develop and any other drug candidates or technologies covered by the asserted third-party patents. In order
to successfully challenge the validity of any such U.S. patent in federal court, we would need to overcome a presumption of validity.
As this burden is a high one requiring us to present clear and convincing evidence as to the invalidity of any such U.S. patent claim,
there is no assurance that a court of competent jurisdiction would invalidate the claims of any such U.S. patent.
If
we are found to infringe, misappropriate or otherwise violate a third party’s intellectual property rights, and we are unsuccessful
in demonstrating that such rights are invalid or unenforceable, we could be required to obtain a license from such a third party in order
to continue developing and marketing our products and technology. However, we may not be able to obtain any required license on commercially
reasonable terms or at all. Even if we were able to obtain a license, it could be or may become non-exclusive, thereby giving our competitors
access to the same technologies licensed to us. We could be forced, including by court order, to cease commercializing the infringing
technology or product. A finding of infringement could prevent us from commercializing our drug candidates or force us to cease some of
our business operations. In the event of a successful claim of infringement against us, we may have to pay substantial damages, including
treble damages and attorneys’ fees for willful infringement, pay royalties and other fees, redesign our infringing drug candidate
or obtain one or more licenses from third parties, which may be impossible or require substantial time and monetary expenditure. Claims
that we have misappropriated the confidential information or trade secrets of third parties could have a similar negative impact on our
business. Any of the foregoing events would harm our business, financial condition, results of operations and prospects.
We may be subject to
claims by third parties asserting that we or our employees have infringed, misappropriated or otherwise violated their intellectual property
rights, or claiming ownership of what we regard as our own intellectual property.
Many
of our employees were previously employed at other biotechnology or pharmaceutical companies. Although we try to ensure that our employees,
consultants and advisors do not use the proprietary information or know-how of others in their work for us, we may be subject to claims
that we or these individuals have used or disclosed intellectual property, including trade secrets or other proprietary information, of
any such individual’s former employer. We may also be subject to claims that patents and applications we have filed to protect inventions
made on our behalf by our employees, consultants and advisors, even those related to one or more of our drug candidates, are rightfully
owned by their former or concurrent employer. Litigation may be necessary to defend against these claims.
If
we fail in prosecuting or defending any such claims, in addition to paying monetary damages, we may lose valuable intellectual property
rights or personnel. Even if we are successful in prosecuting or defending against such claims, litigation could result in substantial
costs, delay development of our drug candidates and be a distraction to management. Any of the foregoing events would harm our business,
financial condition, results of operations and prospects.
We may be subject to
claims challenging the inventorship of our patents and other intellectual property.
We or
our licensors may be subject to claims that former employees, collaborators or other third parties have an interest in our owned or in-licensed
patents, trade secrets, or other intellectual property as an inventor or co-inventor. For example, we or our licensors or collaborators
may have inventorship disputes arising from conflicting obligations of employees, consultants or others who are involved in developing
our drug candidates. While it is our policy to require our employees and contractors who may be involved in the development of intellectual
property to execute agreements assigning such intellectual property to us, we may be unsuccessful in executing such an agreement with
each party who in fact develops intellectual property that we regard as our own. Our and their assignment agreements may not be self-executing
or may be breached, and litigation may be necessary to defend against these and other claims challenging inventorship or our or our licensors’
or collaborators’ ownership of our owned or in-licensed patents, trade secrets or other intellectual property. If we or our licensors
or collaborators fail in defending any such claims, in addition to paying monetary damages, we may lose valuable intellectual property
rights, such as exclusive ownership of, or right to use, intellectual property that is important to our drug candidates. Even if we are
successful in defending against such claims, these claims may create considerable distraction to management and other employees of the
company. Any of the foregoing could have a material adverse effect on our business, financial condition, results of operations and prospects.
Intellectual property
rights do not necessarily address all potential threats.
The
degree of future protection, if any, afforded by our intellectual property rights is uncertain because intellectual property rights have
limitations and may not adequately protect our business or permit us to maintain our competitive advantage. For example:
| · | others may be able to make products that are similar to any drug candidates we may develop or utilize similar technology but that
are not covered by the claims of the patents that we license or may own in the future; |
| · | we, or our current or future licensors or collaborators, might not have been the first to make the inventions covered by the issued
patent or pending patent application that we license or may own in the future; |
| · | we, or our current or future licensors or collaborators might not have been the first to file patent applications covering certain
of our or their inventions; |
| · | others may independently develop similar or alternative technologies or duplicate any of our technologies without infringing our owned
or licensed intellectual property rights; |
| · | it is possible that our pending owned or licensed patent applications or those that we may own or license in the future will not lead
to issued patents; |
| · | issued patents that we hold rights to may be held invalid or unenforceable, including as a result of legal challenges by our competitors; |
| · | our competitors might conduct research and development activities in countries where we do not have patent rights and then use the
information learned from such activities to develop competitive products for sale in our major commercial markets; |
| · | we may not develop additional proprietary technologies that are patentable; |
| · | the intellectual property rights of others may harm our business; and |
| · | we may choose not to file a patent in order to maintain certain trade secrets or know-how, and a third party may subsequently file
a patent directed to such intellectual property. |
Should
any of these events occur, they could harm our business, financial condition, results of operations and prospects.
Intellectual property
litigation may lead to unfavorable publicity that harms our reputation and causes the market price of shares of our Common Stock to decline.
During
the course of any intellectual property litigation, there could be public announcements of the initiation of the litigation as well as
results of hearings, rulings on motions, and other interim proceedings in the litigation. If securities analysts or investors regard these
announcements as negative, the perceived value of our existing products, programs or intellectual property could be diminished. Accordingly,
the market price of shares of our Common Stock may decline. Such announcements could also harm our reputation or the market for our future
products, which could have a material adverse effect on our business.
CAUTIONARY NOTE REGARDING FORWARD-LOOKING STATEMENTS
This prospectus supplement and any accompanying base
prospectus, including the documents incorporated by reference herein, contain “forward-looking statements” within the meaning
of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, that relate
to future events or our future financial performance and involve known and unknown risks, uncertainties and other factors that may cause
our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity,
performance or achievements expressed or implied by these forward-looking statements. Such forward-looking statements concern our anticipated
results and progress of our operations in future periods, planned exploration and, if warranted, development of our properties, plans
related to our business and other matters that may occur in the future. These statements relate to analyses and other information that
are based on forecasts of future results, estimates of amounts not yet determinable and assumptions of management. All statements contained
herein that are not clearly historical in nature are forward-looking, and the words “anticipate,” “believe,” “expect,”
“estimate,” “may,” “will,” “could,” “leading,” “intend,” “contemplate,”
“shall” and similar expressions are generally intended to identify forward-looking statements. Forward-looking statements
are subject to a variety of known and unknown risks, uncertainties and other factors which could cause actual events or results to differ
from those expressed or implied by the forward-looking statements. The section in this prospectus supplement and accompanying prospectus
entitled “Risk Factors” and the sections in our periodic reports, including our Annual Report on Form 10-K for the fiscal
year ended June 30, 2023 (the “2023 Form 10-K”) entitled “Business,” and in the 2023 Form 10-K, the Quarterly
Reports on Form 10-Q for the fiscal quarter ended September 30, 2023 and December 31, 2023, and any future Quarterly Report on Form
10-Qs, entitled “Management’s Discussion and Analysis of Financial Condition and Results of Operations,” as well as
other sections in this prospectus supplement, accompanying prospectus and the documents or reports incorporated by reference into this
prospectus supplement, discuss some of the factors that could contribute to these differences. Forward-looking statements in this prospectus
supplement, the accompanying prospectus and the documents incorporated by reference herein include, but are not limited to, statements
with respect to:
| · | our limited operating history and experience in developing and manufacturing drugs; |
| · | none of our products are approved for commercial sale; |
| · | our substantial capital needs; |
| · | product development risks; |
| · | our lack of sales and marketing personnel; |
| · | our reliance on third parties to conduct our clinical trials; |
| · | regulatory, competitive and contractual risks; |
| · | no assurance that our product candidates will obtain regulatory approval or that the results of clinical studies will be favorable; |
| · | risks related to our intellectual property rights; |
| · | the volatility of the market price and trading volume in our Common Stock; |
| · | the absence of liquidity in our Common Stock; |
| · | the risk of substantial dilution from future issuances of our equity securities; and |
| · | the other risks set forth herein and in the documents incorporated by reference herein under the caption “Risk Factors.” |
The foregoing does not represent an exhaustive list
of matters that may be covered by the forward-looking statements contained herein or risk factors that we are faced with. The factors
set forth above under “Risk Factors” and other cautionary statements made in this prospectus supplement and the accompanying
prospectus should be read and understood as being applicable to all related forward-looking statements wherever they appear in this prospectus
supplement and the accompanying prospectus. The forward-looking statements contained in this prospectus supplement and accompanying prospectus
represent our judgment as of the date of this prospectus supplement and the accompanying prospectus, as applicable. We caution readers
not to place undue reliance on such statements. You should read this prospectus supplement, the accompanying prospectus, and the documents
incorporated by reference herein and therein completely and with the understanding that our actual future results may be materially different
from the plans, intentions and expectations disclosed in the forward-looking statements we make. Except as required by law, we undertake
no obligation to update publicly any forward-looking statements for any reason, even if new information becomes available or other events
occur in the future. All subsequent written and oral forward-looking statements attributable to us or persons acting on our behalf are
expressly qualified in their entirety by the cautionary statements contained above and throughout this prospectus supplement and the accompanying
prospectus.
USE OF PROCEEDS
We estimate that the net proceeds from the sale of our Common Stock, Pre-funded Warrants,
and the Common Warrants in this offering will be approximately $19.0 million, after deducting placement agent fees and estimated
offering expenses payable by us. We intend to use the net proceeds from this offering for working capital and general corporate purposes.
The amount excludes the proceeds, if any, from the exercise of Common Warrants in this offering. If all the Common Warrants sold in this
offering were to be exercised in cash at an exercise price of $1.50 per share, we would receive additional net proceeds of approximately
$15.75 million. We cannot predict when or if these Common Stock Warrants will be exercised. It is possible that these Common Stock Warrants
may expire and never be exercised.
This expected use of the net proceeds from this offering
and our existing cash represents our intentions based upon our current plans, financial condition and business conditions. The amount,
timing and nature of specific expenditures of net proceeds from this offering will depend on a number of factors, including the timing,
scope, progress and results of our development efforts and the timing and progress of any collaboration efforts. As of the date of this
prospectus supplement, we cannot specify with certainty all of the particular uses of the proceeds from this offering. Accordingly, we
will retain broad discretion over the use of such proceeds.
Pending our use of the net proceeds from this offering, we intend to invest
the net proceeds in a variety of capital preservation investments, including short-term, investment-grade, interest-bearing instruments,
and government securities.
DIVIDEND POLICY
We have never declared or paid dividends on our Common
Stock and we do not anticipate paying any cash dividends on our Common Stock in the foreseeable future. Payment of cash dividends, if
any, in the future will be at the discretion of our board of directors and will depend on applicable law and then-existing conditions,
including our financial condition, operating results, contractual restrictions, capital requirements, business prospects and other factors
our board of directors may deem relevant. We currently intend to retain all available funds and any future earnings to fund the development
and growth of our business.
DESCRIPTION
OF SECURITIES WE ARE OFFERING
The
following description is a summary of some of the terms of our securities, our organizational documents and Nevada law. The descriptions
in this prospectus supplement and the accompanying prospectus of our securities and our organizational documents do not purport to be
complete and are subject to, and qualified in their entirety by reference to, our organizational documents, copies of which have been
or will be filed or incorporated by reference as exhibits to the registration statement of which this prospectus supplement and the accompanying
prospectus form a part. This summary supplements the description of our capital stock in the accompanying prospectus and, to the extent
it is inconsistent, replaces the description in the accompanying prospectus.
We are offering 15,000,000 Shares, 6,000,000 Pre-funded Warrants, and 10,500,000
accompanying Common Warrants. The shares of Common Stock or Pre-funded Warrants and accompanying Common Warrants will be issued separately.
We are also registering the shares of Common Stock issuable from time to time upon exercise of the Pre-funded Warrants and Common Warrants
offered hereby.
Common Stock
A description of the Common Stock that we are
offering pursuant to this prospectus supplement is set forth hereunder and under the heading “Description of Capital Stock”
starting on page 8 of the accompanying prospectus. On February 29, 2024, we had 39,924,596 shares of Common Stock outstanding.
Pre-funded Warrants
The following summary of certain terms and
provisions of the Pre-funded Warrants that are being offered hereby is not complete and is subject to, and qualified in its entirety
by, the provisions of the Pre-funded Warrant, the form of which will be filed as an exhibit to a Current Report on Form 8-K that we will
file with the SEC. Prospective investors should carefully review the terms and provisions of the form of Pre-funded Warrant for a complete
description of the terms and conditions of the Pre-funded Warrants.
Term
The Pre-funded Warrants will
not expire until they are fully exercised.
Exercisability
The Pre-funded Warrants are
exercisable at any time until they are fully exercised. The Pre-funded Warrants will be exercisable, at the option of each holder, in
whole or in part by delivering to us a duly executed exercise notice and payment of the exercise price. No fractional shares of Common
Stock will be issued in connection with the exercise of a Pre-funded Warrant. The holder of the Pre-funded Warrant may also satisfy its
obligation to pay the exercise price through a “cashless exercise,” in which the holder receives the net value of the Pre-funded
Warrants in shares of Common Stock determined according to the formula set forth in the Pre-funded Warrant.
Exercise Limitations
Under the terms of the Pre-funded
Warrants, the Company may not effect the exercise of any such warrant, and a holder will not be entitled to exercise any portion of any
such warrant, if, upon giving effect to such exercise, the aggregate number of shares of Common Stock beneficially owned by the holder
(together with its affiliates, any other persons acting as a group together with the holder or any of the holder’s affiliates, and
any other persons whose beneficial ownership of Common Stock would or could be aggregated with the holder’s for purposes of Section
13(d) or Section 16 of the Securities Exchange Act of 1934, as amended) would exceed 4.99% of the number of shares of Common Stock outstanding
immediately after giving effect to the exercise, as such percentage ownership is determined in accordance with the terms of such warrant,
which percentage may be increased or decreased at the holder’s election upon 61 days’ notice to the Company subject to the
terms of such warrants, provided that such percentage may in no event exceed 9.99%.
Exercise Price
The exercise price of our
shares of Common Stock purchasable upon the exercise of the Pre-funded Warrants is $0.0001 per share. The exercise price of the Pre-funded
Warrants and the number of shares of Common Stock issuable upon exercise of the Pre-funded Warrants is subject to appropriate adjustment
in the event of certain stock dividends and distributions, stock splits, stock combinations, reclassifications or similar events affecting
our shares of Common Stock, as well as upon any distribution of assets, including cash, stock or other property, to our stockholders.
Transferability
Subject to applicable laws,
the Pre-funded Warrants may be offered for sale, sold, transferred or assigned without our consent.
Exchange Listing
We do not intend to list
the Pre-funded Warrants on The Nasdaq Capital Market, any other national securities exchange or any other nationally recognized trading
system.
Fundamental Transactions
Upon the consummation of
a fundamental transaction (as described in the Pre-funded Warrants, and generally including any reorganization, recapitalization or reclassification
of our shares of Common Stock, the sale, transfer or other disposition of all or substantially all of our properties or assets, our consolidation
or merger with or into another person, the acquisition of more than 50% of our outstanding shares of Common Stock, or any person or group
becoming the beneficial owner of 50% of the voting power of our outstanding shares of Common Stock), the holders of the Pre-funded Warrants
will be entitled to receive, upon exercise of the Pre-funded Warrants, the kind and amount of securities, cash or other property that
such holders would have received had they exercised the Pre-funded Warrants immediately prior to such fundamental transaction, without
regard to any limitations on exercise contained in the Pre-funded Warrants. Notwithstanding the foregoing, in the event of a fundamental
transaction where the consideration consists solely of cash, solely of marketable securities or a combination of cash and marketable securities,
then each Pre-funded Warrants shall automatically be deemed to be exercised in full in a cashless exercise effective immediately prior
to and contingent upon the consummation of such fundamental transaction.
No Rights as a Stockholder
Except by virtue of such holder’s ownership
of shares of Common Stock, the holder of a Pre-funded Warrant does not have the rights or privileges of a holder of our shares of Common
Stock, including any voting rights, until such holder exercises the Pre-funded Warrant.
Common Warrants
The following summary of certain terms and
provisions of Common Warrants that are being offered hereby is not complete and is subject to, and qualified in its entirety by, the
provisions of the Common Warrants, the form of which will be filed as an exhibit to the registration statement of which this prospectus
forms a part. Prospective investors should carefully review the terms and provisions of the form of Common Warrant for a complete description
of the terms and conditions of the Common Warrants.
Term
The Common Warrants will be immediately exercisable
and will expire on the fifth anniversary of the original issuance date. The exercise price and number of shares of Common Stock issuable
upon exercise is subject to appropriate adjustment in the event of stock dividends, stock splits, reorganizations or similar events affecting
our Common Stock and the exercise price. The Common Warrants will be issued separately from the Shares and Pre-funded Warrants and
may be transferred separately immediately thereafter.
Exercisability
The Common Warrants will be exercisable, at the option
of each holder, in whole or in part, by delivering to us a duly executed exercise notice accompanied by payment in full for the number
of shares of our Common Stock purchased upon such exercise (except in the case of a cashless exercise as discussed below). A holder (together
with its affiliates) may not exercise any portion of any Common Warrant to the extent that the holder would own more than 4.99% of the
outstanding Common Stock immediately after exercise, except that upon at least 61 days’ prior notice from the holder to us, the
holder may increase the amount of ownership of outstanding Common Stock after exercising the holder’s Common Warrants up to 9.99%
of the number of shares of our Common Stock outstanding immediately after giving effect to the exercise, as such percentage ownership
is determined in accordance with the terms of the Common Warrants. No fractional shares of Common Stock will be issued in connection with
the exercise of a Common Warrant. In lieu of fractional shares, we will round up to the next whole share.
Cashless Exercise
If, at the time a holder exercises its Common Warrants,
a registration statement registering the issuance of the shares of Common Stock underlying the Common Warrants under the Securities Act
is not then effective or available and an exemption from registration under the Securities Act is not available for the issuance of such
shares, then in lieu of making the cash payment otherwise contemplated to be made to us upon such exercise in payment of the aggregate
exercise price, the holder may elect instead to receive upon such exercise (either in whole or in part) the net number of shares of Common
Stock determined according to a formula set forth in the Common Warrants.
Exercise Price
Each Common Warrant offered hereby will have an initial
exercise price per share equal to $1.50.
Transferability
Subject to applicable laws, a Common Warrant may be
transferred at the option of the holder upon surrender of the Common Warrant to us together with the appropriate instruments of transfer.
Exchange Listing
There is no established public trading market for
the Common Warrants, and we do not expect a market to develop. In addition, we do not intend to list the Common Warrants on any securities
exchange or nationally recognized trading system. Without an active trading market, the liquidity of the Common Warrants will be limited.
No Rights as a Stockholder
Except as otherwise provided in the Common Warrants
or by virtue of such holder’s ownership of shares of our Common Stock, the holders of the Common Warrants do not have the rights
or privileges of holders of our Common Stock, including any voting rights, until they exercise their Common Warrants.
Anti-Takeover Effects of Our Articles of Incorporation
and Bylaws
Our Articles of Incorporation and Bylaws contain certain provisions that may have anti-takeover
effects, making it more difficult for or preventing a third party from acquiring control of us or changing our board of directors and
management. According to our Articles of Incorporation and Bylaws, neither the holders of our Common Stock nor the holders of any preferred
stock we may issue in the future have cumulative voting rights in the election of our directors. The combination of the present ownership
by a few stockholders of a significant portion of our issued and outstanding Common Stock and lack of cumulative voting makes it more
difficult for other stockholders to replace our board of directors or for a third party to obtain control of us by replacing our board
of directors.
Anti-Takeover Effects of Nevada Law
Business Combinations
The “business combination” provisions
of Sections 78.411 to 78.444, inclusive, of the Nevada Revised Statutes (“NRS”) generally prohibit a Nevada corporation with
at least 200 stockholders from engaging in various “combination” transactions with any interested stockholder for a period
of two years after the date of the transaction in which the person became an interested stockholder, unless the transaction is approved
by the board of directors prior to the date the interested stockholder obtained such status or the combination is approved by the board
of directors and thereafter is approved at a meeting of the stockholders by the affirmative vote of stockholders representing at least
60% of the outstanding voting power held by disinterested stockholders, and extends beyond the expiration of the two-year period, unless:
|
● |
the combination was approved by the board of directors prior to the person becoming an interested stockholder or the transaction by which the person first became an interested stockholder was approved by the board of directors before the person became an interested stockholder or the combination is later approved by a majority of the voting power held by disinterested stockholders; or |
|
● |
if the consideration to be paid by the interested stockholder is at least equal to the highest of: (a) the highest price per share paid by the interested stockholder within the two years immediately preceding the date of the announcement of the combination or in the transaction in which it became an interested stockholder, whichever is higher, (b) the market value per share of Common Stock on the date of announcement of the combination and the date the interested stockholder acquired the shares, whichever is higher, or (c) for holders of preferred stock, the highest liquidation value of the preferred stock, if it is higher. |
A “combination” is generally defined to
include mergers or consolidations or any sale, lease exchange, mortgage, pledge, transfer, or other disposition, in one transaction or
a series of transactions, with an “interested stockholder” having: (a) an aggregate market value equal to 5% or more of the
aggregate market value of the assets of the corporation, (b) an aggregate market value equal to 5% or more of the aggregate market value
of all outstanding shares of the corporation, (c) 10% or more of the earning power or net income of the corporation, and (d) certain other
transactions with an interested stockholder or an affiliate or associate of an interested stockholder.
In general, an “interested stockholder”
is a person who, together with affiliates and associates, owns (or within two years, did own) 10% or more of a corporation’s voting
stock. The statute could prohibit or delay mergers or other takeover or change in control attempts and, accordingly, may discourage attempts
to acquire our Company even though such a transaction may offer our stockholders the opportunity to sell their stock at a price above
the prevailing market price.
Control Share Acquisitions
The “control share” provisions of Sections
78.378 to 78.3793, inclusive, of the NRS apply to “issuing corporations” that are Nevada corporations with at least 200 stockholders,
including at least 100 stockholders of record who are Nevada residents, and that conduct business directly or indirectly in Nevada. The
control share statute prohibits an acquirer, under certain circumstances, from voting its shares of a target corporation’s stock
after crossing certain ownership threshold percentages, unless the acquirer obtains approval of the target corporation’s disinterested
stockholders. The statute specifies three thresholds: one-fifth or more but less than one-third, one-third but less than a majority, and
a majority or more, of the outstanding voting power. Generally, once an acquirer crosses one of the above thresholds, those shares in
an offer or acquisition and acquired within 90 days thereof become “control shares” and such control shares are deprived of
the right to vote until disinterested stockholders restore the right. These provisions also provide that if control shares are accorded
full voting rights and the acquiring person has acquired a majority or more of all voting power, all other stockholders who do not vote
in favor of authorizing voting rights to the control shares are entitled to demand payment for the fair value of their shares in accordance
with statutory procedures established for dissenters’ rights.
A corporation may elect to not be governed by, or “opt out” of, the control
share provisions by making an election in its articles of incorporation or bylaws, provided that the opt-out election must be in place
on the 10th day following the date an acquiring person has acquired a controlling interest, that is, crossing any of the three
thresholds described above. We have not opted out of the control share statutes, and will be subject to these statutes if we are an “issuing
corporation” as defined in such statutes.
The effect of the Nevada control share statutes is that the acquiring person, and those acting in association with
the acquiring person, will obtain only such voting rights in the control shares as are conferred by a resolution of the stockholders at
an annual or special meeting. The Nevada control share law, if applicable, could have the effect of discouraging takeovers of our Company.
DILUTION
If you invest in this offering, your ownership interest
will be diluted to the extent of the difference between the public offering price per share and the as adjusted net tangible book value
per Common Stock immediately after this offering.
Our net tangible book value as of December 31, 2023
was approximately $6.6 million, or $0.16 per share of Common Stock. Net tangible book value per share is determined by dividing our total
tangible assets, less total liabilities, by the number of shares of our Common Stock outstanding as of December 31, 2023.
After giving effect to the sale of the Shares and
Pre-funded Warrants and the accompanying Common Warrants in this offering at the combined public offering price of $1.00 per Share and
$ 0.9999 per Pre-funded Warrant, and after deducting placement agent fees and estimated offering expenses payable by us, our as adjusted
net tangible book value as of December 31, 2023 would have been approximately $25.2 million, or approximately $0.42 per share of Common
Stock. This represents an immediate increase in the as adjusted net tangible book value of approximately $0.25 per share to our existing
stockholders and an immediate dilution in as adjusted net tangible book value of approximately $0.58 per share to new investors in this
offering.
The following table illustrates this per share dilution.
Combined public offering price per Share or Pre-funded Warrant and accompanying Common Warrants |
|
|
|
|
|
$ |
1.00 |
|
Historical net tangible book value per share as of December 31, 2023 |
|
$ |
0.16 |
|
|
|
|
|
Increase in net tangible book value per share attributable to this offering |
|
$ |
0.25 |
|
|
|
|
|
As adjusted net tangible book value per share as of December 31, 2023, after giving effect to this offering |
|
|
|
|
|
$ |
0.42 |
|
Dilution per share to new investors in this offering |
|
|
|
|
|
$ |
0.58 |
|
The number of shares of Common Stock to be outstanding immediately after this offering
is based on 36,428,949 shares of our Common Stock outstanding as of December 31, 2023, and excludes:
| · | 4,173,325 shares of Common Stock issuable upon the exercise of outstanding stock options at a weighted
average exercise price of $6.84 per share; |
| · | 7 ,770,285 shares of Common Stock issuable upon the exercise of outstanding and exercisable warrants at
a weighted average exercise price of $2.06 per share (which weighted average exercise price would decrease to $1.29 per share as a result
of the adjustment to the exercise price of the Acuitas Warrants following this offering (See Risk Factors – You may experience future
dilution as a result of future equity offerings or if we issue shares subject to options, warrants, stock awards or other arrangements.); |
| · | 687,428 shares of Common Stock issuable upon vesting of restricted stock units issued under our equity
incentive plan; |
| · | 4,384 shares of Common Stock issued pursuant to the ATM Agreement between the Company and Cantor since
December 31, 2023; |
| · | 1,050,000 shares of Common Stock issuable upon exercise of the Placement
Agent’s Warrants; and |
| · | 10,500,000 shares of Common Stock issuable upon exercise of the Common
Warrants.
|
Except as otherwise indicated, all information in this prospectus supplement assumes
no exercise, conversion, or settlement of the outstanding options, preferred stock, or warrants described above, no exercise of Common
Warrants issued and sold in this offering, and no exercise of the Placement Agent’s Warrants. To the extent that any of these outstanding
warrants or options are exercised at prices per share below the public offering price per share in this offering or we issue additional
shares under our equity incentive plans at prices below the public offering price per share in this offering, you may experience further
dilution. In addition, to the extent that we raise additional capital by issuing equity or convertible debt securities, your ownership
will be further diluted.
PLAN OF DISTRIBUTION
We have engaged ThinkEquity LLC, or the placement
agent, to act as our exclusive placement agent to solicit offers to purchase the Shares and/or Pre-funded Warrants and accompanying Common
Warrants offered by this prospectus. The placement agent is not purchasing or selling any such securities, nor is it required to
arrange for the purchase and sale of any specific number or dollar amount of such securities, other than to use its “reasonable
best efforts” to arrange for the sale of such securities by us. Therefore, we may not sell all of the Shares and/or pre-funded
warrants and accompanying Common Warrants being offered. The terms of this offering are subject to market conditions and negotiations
between us, the placement agent and prospective investors. The placement agent will have no authority to bind us by virtue of their placement
agency agreement. This is a best efforts offering and there is no minimum offering amount required as a condition to the closing of this
offering. The placement agent may retain sub-agents and selected dealers in connection with this offering.
Investors purchasing securities offered hereby will
have the option to execute a securities purchase agreement with us. Investors who do not enter
into a securities purchase agreement shall rely solely on this prospectus in connection with the purchase of our securities in this offering. In
addition to rights and remedies available to all purchasers in this offering under federal securities and state law, the purchasers which
enter into a securities purchase agreement will also be able to bring claims of breach of contract against us.
Delivery of the shares of Common Stock, Pre-funded
Warrants and the Common Warrants offered hereby is expected to occur on or about March 6, 2024, subject to satisfaction of certain customary
closing conditions.
Fees and Expenses
The following table shows the per share price and
total cash fees we will pay to the placement agent in connection with the sale of the securities pursuant to this prospectus.
| |
Per Share of Common Stock and Accompanying Common Warrant | |
Per Pre-Funded Warrant and Accompanying Common Warrant |
Offering price |
|
$ |
1.000 |
|
|
$ |
0.9999 |
|
Placement agent commissions (7.5%) | |
$ | 0.075 | | |
$ | 0.7499 | |
Proceeds, before expense, to us | |
$ | 0.925 | | |
$ | 0.9249 | |
We have agreed to pay a non-accountable expense allowance
to the placement agent equal to 1% of the gross proceeds received in this offering.
We have paid an expense deposit of $50,000 to the
placement agent, which will be applied against the out-of-pocket accountable expenses that will be paid by us to the placement agent in
connection with this offering, and will be reimbursed to us to the extent not actually incurred in compliance with Rule 5110(g)(4)(A)
of the Financial Industry Regulatory Authority (“FINRA”).
We have also agreed to pay certain of the placement
agent’s expenses relating to the offering, including: (a) all fees, expenses and disbursements relating to background checks of
our officers, directors and entities in an amount not to exceed $15,000 in the aggregate; (b) fees and expenses of the placement agent’s
legal counsel not to exceed $125,000; (c) a $29,500 cost associated with the placement agent use of Ipreo’s book-building, prospectus
tracking and compliance software for the offering; (d) $10,000 for data services and communications expenses; (e) up to $30,000 of market
making and trading, and clearing firm settlement expenses for the offering; (f) up to $10,000 of the placement agent’s actual accountable
“road show” expenses; and (g) the costs associated with bound volumes of the public offering materials as well as commemorative
mementos and lucite tombstones.
Our total estimated expenses of the offering, including registration, filing and
listing fees, printing fees and legal and accounting expenses, but excluding placement agent fees and excluding the non-accountable expense
allowance, are approximately $450,000.
Placement Agent’s Warrants
Upon closing of this offering, we have agreed to issue the placement agent warrants (“Placement
Agent’s Warrants”) to purchase up to 1,050,000 shares of Common Stock (5% of the aggregate number of shares of Common Stock
and Pre-funded Warrants sold in this offering). The Placement Agent’s Warrants will be exercisable at a per share exercise price
equal $1.25, which is equal to 125% of the public offering price per share in this offering. The Placement Agent’s Warrants are
exercisable at any time and from time to time, in whole or in part, during the five-year period commencing 180 days from the commencement
of sales of the Shares and Pre-funded Warrants and the Common Warrants in this offering.
The Placement Agent’s Warrants have been deemed compensation by FINRA and are therefore
subject to a 180-day lock-up pursuant to Rule 5110(e)(1)(A) of FINRA. The placement agent (or permitted assignees under Rule 5110(e)(2))
will not sell, transfer, assign, pledge, or hypothecate these warrants or the securities underlying these warrants, nor will they engage
in any hedging, short sale, derivative, put, or call transaction that would result in the effective economic disposition of the warrants
or the underlying securities for a period of 180 days following the commencement of sales of the securities issued in this offering. In
addition, the Placement Agent’s Warrants provide for registration rights upon request, in certain cases. The sole demand registration
right provided will not be greater than five years from the commencement of sales of the securities issued in this offering in compliance
with FINRA Rule 5110(g)(8)(C). The piggyback registration rights provided will not be greater than seven years from the commencement of
sales of the securities issued in this offering in compliance with FINRA Rule 5110(g)(8)(D). We will bear all fees and expenses attendant
to registering the securities issuable on exercise of the warrants other than underwriting commissions incurred and payable by the holders.
The exercise price and number of shares issuable upon exercise of the Placement Agent’s Warrants may be adjusted in certain circumstances
including in the event of a stock dividend or our recapitalization, reorganization, merger or consolidation. However, the Placement Agent’s
Warrant exercise price or underlying shares will not be adjusted for issuances of shares of Common Stock at a price below the warrant
exercise price.
Lock-Up Agreements
Pursuant to
“lock-up” agreements, we and our executive officers, directors and affiliates have agreed, for a period of 90 days from the
date of this prospectus supplement not to, directly or indirectly, offer to sell, sell, pledge or otherwise transfer or dispose of any
of shares of (or enter into any transaction or device that is designed to, or could be expected to, result in the transfer or disposition
by any person at any time in the future of) our Common Stock, enter into any swap or other derivatives transaction that transfers to another,
in whole or in part, any of the economic benefits or risks of ownership of shares of our Common Stock, make any demand for or exercise
any right or cause to be filed a registration statement, including any amendments thereto, with respect to the registration of any shares
of Common Stock or securities convertible into or exercisable or exchangeable for shares of Common Stock or any other of our securities
or publicly disclose the intention to do any of the foregoing, subject to customary exceptions, without the prior written consent of the
placement agent. We have also agreed to a covenant to not enter into variable rate financings for a period of 90 days following
the closing of the offering.
Right of First Refusal
We have granted the placement
agent an irrevocable right of first refusal (the "Right of First Refusal"), for a period of 14 months after the date the Offering
is completed for aggregate net proceeds of not less than $10 million, to act, except as set forth below, as sole investment banker, sole
book-runner and/or sole placement agent, at the placement agent’s sole discretion, for each and every future public and private
equity offering that is not an “at-the-market” offering (an “ATM”) (an ATM executed through a broker dealer as
sales agent), and sole investment banker, sole book-runner and/or sole placement agent, at the Placement Agent’s sole discretion,
for each and every future debt offering (such future public and private equity offering or debt offering, a “Future Offering”),
including all equity linked financings, during such fourteen (14) month period for the Company, or any successor to or any subsidiary
of the Company, on reasonable and customary terms, provided a Future Offering shall not be deemed to include, and no Right of First Refusal
is granted to the placement agent in connection with, any of the following: (a) any equity securities directly issued by the Company pursuant
to acquisitions or strategic transactions, including as part of any grant funding from a third party, or (b) any offer or sale of equity
securities by the Company directly to non-U.S. persons domiciled in the following jurisdictions: China, Korea, Latin America (e.g. the
Caribbean and/or the Cayman Islands) and Middle East, in each case, in a private placement not otherwise involving a public offering.
Notwithstanding anything to the contrary set forth above, the placement agent acknowledges that the Company is subject to a pre-existing
agreement with a third party under which such third party has a right of first refusal to act as the co-lead bookrunning underwriter,
co-lead initial purchaser, co-lead placement agent or co-lead selling agent, as the case may be, on any financing involving equity securities
for the Company (the “Prior ROFR”). In case the placement agent wishes to exercise its Right of First Refusal hereunder, the
Company will use its commercially reasonable efforts to obtain a waiver of the Prior ROFR, subject to certain conditions.
Prior Relationships
The placement agent acted as the representative of
the underwriters for our public offering that closed in August 2021. The placement agent received a commission equal to 4% of the gross
proceeds of our initial public offering, and a 1% non-accountable expense allowance.
Regulation M Compliance
The placement agent may be deemed to be an underwriter
within the meaning of Section 2(a)(11) of the Securities Act, and any commissions received by it and any profit realized on the sale of
our securities offered hereby by it while acting as principal might be deemed to be underwriting discounts or commissions under the Securities
Act. The placement agent will be required to comply with the requirements of the Securities Act and the Exchange Act, including, without
limitation, Rule 10b-5 and Regulation M under the Exchange Act. These rules and regulations may limit the timing of purchases and sales
of our securities by the placement agent. Under these rules and regulations, the placement agent may not (i) engage in any stabilization
activity in connection with our securities; and (ii) bid for or purchase any of our securities or attempt to induce any person to purchase
any of our securities, other than as permitted under the Exchange Act, until they have completed their participation in the distribution.
Indemnification
We have agreed to indemnify the placement agent against
certain liabilities, including liabilities under the Securities Act and liabilities arising from breaches of representations and warranties
contained in our placement agency agreement with the placement agent. We have also agreed to contribute to payments the placement agent
may be required to make in respect of such liabilities.
Nasdaq Capital Market Listing
Our Common Stock is listed on The Nasdaq Capital Market
under the symbol “BIVI.” There is no established trading market for the Pre-funded Warrants and we do not intend to list the
Pre-funded Warrants on any securities exchange or nationally recognized trading system.
Other
From time to time, the placement agent and/or their
affiliates may in the future provide, various investment banking and other financial services for us for which they may receive customary
fees. In the course of their businesses, the placement agent and their affiliates may actively trade our securities or loans for their
own account or for the accounts of customers, and, accordingly, the placement agent and their affiliates may at any time hold long or
short positions in such securities or loans.
Except for services provided in connection with this
offering and our initial public offering in which the placement agent acted as sole underwriter, the placement agent has not provided
any investment banking or other financial services to us during the 180-day period preceding the date of this prospectus supplement.
LEGAL MATTERS
The validity of the shares Common Stock and the shares of Common Stock underlying
the Pre-funded Warrants and the Common Warrants offered hereby will be passed upon for us by Sherman & Howard L.L.C. Certain legal
matters related to the offering and the validity of the Pre-funded Warrants and Common Warrants will be passed upon for us by Reed Smith
LLP, New York, New York. Certain legal matters related to the offering will be passed upon for the placement agent by Sheppard, Mullin,
Richter & Hampton LLP, New York, New York.
EXPERTS
The balance sheets of BioVie Inc. as of June 30, 2023
and 2022, and the related statements of operations and comprehensive loss, changes in stockholders’ equity, and cash flows for each
of the years then ended, have been audited by EisnerAmper LLP, independent registered public accounting firm, as stated in their report
which is incorporated by reference, which report includes an explanatory paragraph about the existence of substantial doubt concerning
the Company’s ability to continue as a going concern. Such financial statements have been incorporated by reference in reliance
on the report of such firm given upon their authority as experts in accounting and auditing.
WHERE YOU CAN FIND MORE INFORMATION
This prospectus supplement and accompanying base prospectus
is part of the registration statement on Form S-3 we filed with the SEC under the Securities Act and does not contain all the information
set forth in the registration statement. Whenever a reference is made in this prospectus supplement or the accompanying base prospectus
to any of our contracts, agreements or other documents, the reference may not be complete and you should refer to the exhibits that are
a part of the registration statement or the exhibits to the reports or other documents incorporated by reference into this prospectus
supplement for a copy of such contract, agreement or other document. Because we are subject to the information and reporting requirements
of the Exchange Act, we file annual, quarterly and current reports, proxy statements and other
information with the SEC. Our SEC filings are available to the public over the internet at the SEC’s website at http://www.sec.gov.
You may also access our SEC filings at our website
https://bioviepharma.com/. Our website and the information contained on, or that can be accessed through, our website will not
be deemed to be incorporated by reference in, and are not considered part of, this prospectus supplement. You should not rely on our website
or any such information in making your decision whether to purchase our securities.
INCORPORATION OF CERTAIN INFORMATION BY REFERENCE
The SEC allows us to incorporate by reference into
this prospectus supplement the information contained in other documents we file with the SEC, which means that we can disclose important
information to you by referring you to those documents. Any statement contained in any document incorporated or deemed to be incorporated
by reference herein shall be deemed to be modified or superseded, for purposes of this prospectus supplement, to the extent that a statement
contained in or omitted from this prospectus supplement, or in any other subsequently filed document that also is or is deemed to be incorporated
by reference herein, modifies or supersedes such statement. Any such statement so modified or superseded shall not be deemed, except as
so modified or superseded, to constitute a part of this prospectus supplement. We incorporate by reference the documents listed below
which have been filed by us:
| · | Our Annual Report on Form 10-K for the year ended June 30, 2023, filed with the SEC on August 16, 2023, including those portions of
the Form 10-K incorporated by reference from our definitive proxy statement filed with the SEC on September 29, 2023, including any amendments
or supplements thereto; |
| · | Our Quarterly Report on Form 10-Q for the period ended September 30, 2023, filed with the SEC on November 8, 2023; |
| · | Our Quarterly Report on Form 10-Q for the period ended December 31, 2023, filed with the SEC on February 13, 2024; |
| · | Our Current Reports on Form 8-K, filed with the SEC on October 25, 2023, November 13,
2023, November 29, 2023, January 19, 2024, January 25, 2024, March 1, 2024, March 4, 2024; and |
| · | The description of our Common Stock contained in our registration on Form 8-A (File No. 001-39015) filed with the SEC on August 25,
2020, including any amendment or report filed for the purpose of updating such description. |
All documents we file with the SEC pursuant to Sections
13(a), 13(c), 14 or 15(d) of the Exchange Act, except as to any portion of any report or documents that is not deemed filed under such
provisions, (1) on or after the date of filing of the registration statement containing this prospectus supplement and prior to the effectiveness
of the registration statement and (2) on or after the date of this prospectus supplement until the earlier of the date on which all of
the securities registered hereunder have been sold or the registration statement of which this prospectus supplement is a part has been
withdrawn, shall be deemed incorporated by reference in this prospectus supplement and to be a part of this prospectus supplement from
the date of filing of those documents and will be automatically updated and, to the extent described above, supersede information contained
or incorporated by reference in this prospectus supplement and previously filed documents that are incorporated by reference in this prospectus
supplement.
Nothing in this prospectus supplement shall be deemed
to incorporate information furnished but not filed with the SEC pursuant to Item 2.02, 7.01 or 9.01 of Form 8-K. Upon written or oral
request, we will provide without charge to each person, including any beneficial owner, to whom a copy of the prospectus is delivered
a copy of any or all of the reports or documents incorporated by reference herein (other than exhibits to such documents, unless such
exhibits are specifically incorporated by reference herein). You may request a copy of these filings, at no cost, by writing or telephoning
us at the following address: BioVie Inc., 680 W Nye Lane, Suite 204, Carson City, NV 89703.
PROSPECTUS |
Filed
Pursuant to Rule 424(b)(3)
|
|
File
No. 333-274083
|
Primary
Offering of
$300,000,000
Class
A Common Stock
Preferred
Stock
Warrants
Debt
Securities
Rights
Units
and
Secondary
Offering of
Up
to 311,002 Shares of Class A Common Stock Offered by the Selling Stockholders
This
prospectus relates to the offer and sale, from time to time, by BioVie Inc. (we, us, or the Company),
in one or more offerings, any combination of Class A common stock (as defined below), preferred stock, warrants, debt securities, rights
to purchase Class A common stock or other securities or units having a maximum aggregate offering price of $300,000,000. When we decide
to sell a particular class or series of securities, we will provide specific terms of the offered securities in a prospectus supplement.
This
prospectus also relates to the offer and resale, from time to time, by the selling stockholders named under the heading Selling
Stockholders in this prospectus (the Selling Stockholders), and their donees, pledgees, transferees or other successors-in-interest,
of up to 311,002 shares (the Shares) of common stock, par value $0.0001 per share (the Class A common stock),
of the Company, issuable upon the exercise of the warrants to purchase 311,002 shares of Class A common stock at an exercise price per
share equal to $5.82 (the Lender Warrants) held by the Selling Stockholders. We are registering the offer and sale of the
Shares issuable upon exercise of the Lender Warrants held by the Selling Stockholders to satisfy the registration rights they were granted
by the Company pursuant to the Loan and Security Agreement and the Supplement to the Loan and Security Agreement, each entered into on
November 30, 2021 (together, the Loan Agreement) with Avenue Venture Opportunities Fund II, L.P. (AVOPII)
and Avenue Venture Opportunities Fund, L.P. (AVOPI and, together with AVOPII, the Lenders).
Discounts,
concessions, commissions and similar selling expenses attributable to the sale of Shares covered by this prospectus will be borne by
the Selling Stockholders. We will pay all expenses (other than discounts, concessions, commissions and similar selling expenses) relating
to the registration of the Shares with the Securities and Exchange Commission (the SEC).
The
prospectus supplements may also add, update or change information contained in or incorporated by reference into this prospectus. However,
no prospectus supplement shall offer a security that is not registered and described in this prospectus at the time of its effectiveness. You should read this prospectus and any prospectus supplement, as well as the documents incorporated by reference or deemed to be incorporated
by reference into this prospectus, carefully before you invest. This prospectus may not be used to offer or sell our securities unless
accompanied by a prospectus supplement relating to the offered securities.
Our Class A common stock is listed on the Nasdaq
Capital Market under the symbol “BIVI.” On August 25, 2023, the closing price for our Common Stock, as reported on The Nasdaq
Capital Market was $3.37 per share. Each prospectus supplement will contain information, where applicable, as to our listing on the Nasdaq
Capital Market or on any other securities exchange of the securities covered by the prospectus supplement.
These
securities may be sold directly by us, through dealers or agents designated from time to time, to or through underwriters or through
a combination of these methods. Additionally, the Selling Stockholders may sell or otherwise dispose of the Shares covered by this prospectus
in a number of different ways and at varying prices. See Plan of Distribution in this prospectus. We may also describe
the plan of distribution for any particular offering of our securities in a prospectus supplement. If any agents, underwriters or dealers
are involved in the sale of any securities in respect of which this prospectus is being delivered, we will disclose their names and the
nature of our arrangements with them in a prospectus supplement. The net proceeds we expect to receive from any such sale will also be
included in a prospectus supplement.
We
will not receive any proceeds from the sales of Shares by the Selling Stockholders. Upon any exercise of the Lender Warrants by payment
of cash, we will receive the cash exercise price paid by the holders of the Lender Warrants. We intend to use those proceeds, if any,
for working capital and general corporate purposes.
An
investment in our securities involves a high degree of risk. Please carefully read the information under the headings Risk
Factors beginning on page 5 of this prospectus, the applicable prospectus supplement and Item 1A – Risk
Factors of our most recent Annual Report on Form 10-K and in any Quarterly Report on Form 10-Q that is incorporated by
reference in this prospectus before you invest in our securities.
We
may amend or supplement this prospectus from time to time by filing amendments or supplements as required. You should read the entire
prospectus and any amendments or supplements carefully before you make your investment decision.
Neither
the SEC nor any state securities commission has approved or disapproved of these securities or determined if this prospectus is truthful
or complete. Any representation to the contrary is a criminal offense.
The
date of this prospectus is August 28, 2023
TABLE
OF CONTENTS
ABOUT
THIS PROSPECTUS
This
prospectus is part of a Registration Statement that we filed with the SEC using a shelf registration process. Under this
shelf registration process, we may offer from time to time securities having a maximum aggregate offering price of $300,000,000. In addition,
the Selling Stockholders may from time to time sell up to an aggregate of 311,002 shares of Class A common stock issuable upon exercise
of the Lender Warrants. Each time we or the Selling Stockholders offer any type or series of securities under this prospectus, we will
prepare and file with the SEC a prospectus supplement that contains more specific information about the terms of that offering. We may
also authorize one or more free writing prospectuses to be provided to you that may contain material information relating to these offerings. The
prospectus supplement and any related free writing prospectus that we may authorize to be provided to you may also add, update or change
information contained in this prospectus or the documents incorporated herein by reference. You should read carefully both this prospectus,
any prospectus supplement and any related free writing prospectuses we have authorized for use in connection with a specific offering,
together with additional information described below under the caption Where You Can Find More Information, before
buying any of the securities being offered.
This
prospectus does not contain all the information provided in the Registration Statement we filed with the SEC. For further information
about us or our securities offered hereby, you should refer to that Registration Statement, which you can obtain from the SEC as described
below under Where You Can Find More Information.
Neither
we nor the Selling Stockholders have authorized anyone to provide any information other than that contained or incorporated by reference
in this prospectus or in any applicable prospectus supplement or any applicable free writing prospectus that we have authorized. We take
no responsibility for and can provide no assurance as to the reliability of, any other information that others may give you. The securities
offered hereby are not being offered in any jurisdiction where the offer is not permitted. You should not assume that the information
contained in or incorporated by reference in this prospectus is accurate as of any date other than the respective dates of such document.
Our business, financial condition, results of operations and prospects may have changed since those dates.
We
and the Selling Stockholders may sell securities through underwriters or dealers, through agents, directly to purchasers or through any
combination of these methods. We and our agents reserve the sole right to accept or reject in whole or in part any proposed purchase
of securities. The prospectus supplement, which we will prepare and file with the SEC each time we offer securities, will set forth the
names of any underwriters, agents or others involved in the sale of securities, and any applicable fee, commission or discount arrangements
with them. See Plan of Distribution.
Unless
the context otherwise indicates, references in this prospectus to, BioVie, the Company, we,
our, or us mean BioVie, Inc., a Nevada corporation. The term Selling Stockholders refers, collectively,
to the selling stockholders named under the heading Selling Stockholders in this prospectus and their donees, pledgees,
transferees or other successors-in-interest.
PROSPECTUS
SUMMARY
This
prospectus summary highlights certain information about our company and other information contained elsewhere in this prospectus or in
documents incorporated by reference. This summary does not contain all of the information that you should consider before making an investment
decision. You should carefully read the entire prospectus, any prospectus supplement, including the matters set forth under the section
of this prospectus entitled Risk Factors and the financial statements and related notes and other information that we incorporate
by reference herein, including our Annual Report on Form 10-K and our Quarterly Reports on Form 10-Q, before making an investment
decision.
Our
Company
We
are a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders and
advanced liver disease.
Neurodegenerative
Disease Program
In neurodegenerative disease, the Company’s
drug candidate NE3107 inhibits inflammatory activation of extracellular single-regulated kinase (“ERK”) and Nuclear factor
kappa-light-chain-enhancer of activated B cells (“NFkB”) (e.g., tumor necrosis factor (“TNF”) signaling) that
leads to neuroinflammation and insulin resistance, but not their homeostatic functions (e.g., insulin signaling and neuron growth and
survival). Both inflammation and insulin resistance are drivers of Alzheimer’s disease (“AD”) and Parkinson’s
disease (“PD”).
The Company is conducting a potentially pivotal Phase 3 randomized, double
blind, placebo controlled, parallel group, multicenter study to evaluate NE3107 in patients who have mild to moderate AD (NCT04669028).
The study has co-primary endpoints looking at cognition using the Alzheimer’s Disease Assessment Scale-Cognitive Scale (ADAS-Cog
12) and function using the Alzheimer’s Disease Cooperative Study-Clinical Global Impression of Change (ADCS-CGIC). The program is
fully enrolled and is targeting primary completion in the fourth quarter of the calendar 2023 year.
In
December 2022, topline results were released from the Companys Phase 2 study assessing NE3107s safety and tolerability
and potential pro-motoric impact in PD patients. The NM201 study (NCT05083260) was a double-blind, placebo-controlled, safety, tolerability,
and pharmacokinetics study in PD participants treated with carbidopa/levodopa and NE3107. Forty-five patients with a defined L-dopa off
state were randomized 1:1 to placebo:NE3107 20 mg twice daily for 28 days. The trial was launched with two design objectives:
1) the primary objective was safety and a drug-drug interaction study (as requested by the U.S. Food and Drug Administration (FDA))
to demonstrate the absence of adverse interactions of NE3107 with levodopa; and 2) the secondary objective was to determine if preclinical
indications of promotoric activity and apparent enhancement of levodopa activity observed in a Parkinsons disease model in monkeys
can be seen in humans. Both objectives of the study were met. Patients treated with NE3107 experienced greater motor control.
The
Company provided the financial support and the use of our NE3107 formulated drug product for an open-label phase 2, Investigator-Initiated
Trial in mild cognitive impairment (MCI) and Mild AD, NCT05227820, conducted by (The Regenesis Project) of
Sheldon Jordan. The study received FDA authorization on December 12, 2021, and was designed to measure NE3107s effect on cognition,
cerebral spinal fluid (CSF) and blood biomarkers, and neuro-imagining endpoints. Topline results were released September
7, 2022, and additional data was presented at the Clinical Trial in Alzheimers Disease (CTAD) annual conference
in December 2022. The data showed that three months of treatment with NE3107 in patients with MCI and mild AD enhanced cognition compared
to baseline, as measured using multiple rating scales, had improvement in daily function and improvements in inflammation correlated
with improved cognition. No drug-related adverse events were observed.
The
Company acquired the biopharmaceutical assets of NeurMedix, Inc. (NeurMedix), from a related party privately held clinical-stage
pharmaceutical company, in June 2021. The acquired assets included NE3107, a potentially selective inhibitor of inflammatory ERK signaling
that, based on animal studies and Dr. Jordans study, is believed to reduce neuroinflammation. NE3107 is a novel orally administered
small molecule that is thought to inhibit inflammation-driven insulin resistance and major pathological inflammatory cascades with a
novel mechanism of action. There is emerging scientific consensus that both inflammation and insulin resistance may play fundamental
roles in the development of AD and PD, and NE3107 could, if approved by the FDA represent a new medical approach to treating these devastating
conditions affecting an estimated 6 million Americans suffering from AD and 1 million Americans suffering from PD.
Inflammation-driven
insulin resistance is believed to be implicated in a broad range of serious diseases, and we plan to begin exploring these opportunities
in the coming months using NE3107 or related compounds acquired in the NeurMedix asset purchase. NE3107 is patented in the United States
(U.S.), Australia, Canada, Europe and South Korea.
Liver
Disease Program
In
liver disease, our Orphan Drug candidate BIV201 (continuous infusion terlipressin), with FDA Fast Track status, has been evaluated in
a U.S. Phase 2b study (NCT04112199) for the treatment of refractory ascites due to liver cirrhosis. BIV201 is administered as a patent-pending
liquid formulation. The study was closed before full enrollment, without clinically meaningful adverse effects associated with BIV201
treatment and data that appeared to show that treatment with BIV201 plus standard-of-care (SOC) resulted in a reduction
in ascites fluid accumulation during treatment versus pre-treatment. In June 2023, we requested guidance from the FDA regarding the design
and endpoints for definitive clinical testing of BIV201 for the treatment of ascites due to chronic liver cirrhosis.
While
the active agent, terlipressin, is approved in the U.S. and in about 40 countries for related complications of advanced liver cirrhosis,
treatment of ascites is not included in these authorizations. Patients with refractory ascites suffer from frequent life-threatening
complications, generate more than $5 billion in annual treatment costs, and have an estimated 50% mortality rate within 6 to 12 months.
The U.S. FDA has not approved any drug to treat refractory ascites.
The
BIV201 development program was initiated by LAT Pharma LLC. On April 11, 2016, the Company acquired LAT Pharma LLC and the rights to
its BIV201 development program. The Company currently owns all development and marketing rights to this drug candidate. Pursuant to the
Agreement and Plan of Merger entered into on April 11, 2016, between our predecessor entities, LAT Pharma LLC and NanoAntibiotics, Inc.,
BioVie is obligated to pay a low single digit royalty on net sales of BIV201 (continuous infusion terlipressin) to be shared among LAT
Pharma Members, PharmaIn Corporation, and The Barrett Edge, Inc.
The
Securities We May Offer
This
prospectus is part of a Registration Statement that we filed with the SEC utilizing a shelf registration process. Under this shelf registration
process, we may sell any combination of:
| ● | debt
securities, in one or more series; |
| ● | right
to purchase common stock or other securities; and/or |
in
one or more offerings up to a total dollar amount of $300,000,000. This prospectus provides you with a general description of the securities
we may offer. Each time we sell securities, we will provide a prospectus supplement that will contain specific information about the
terms of that specific offering and include a discussion of any risk factors or other special considerations that apply to those securities.
The prospectus supplement may also add, update or change information contained in this prospectus. You should read both this prospectus
and any prospectus supplement together with the additional information described under the heading Where You Can Find More Information.
Securities
Offered by the Selling Securityholders
This
prospectus also relates to the resale from time to time by the Selling Stockholders identified in this prospectus of up to 311,002 shares
of Class A common stock issuable upon the exercise of the Lender Warrants held by the Selling Stockholders. We are registering the offer
and sale of the Shares to satisfy the registration rights they were granted by the Company pursuant to the Loan Agreement.
On
November 30, 2021 (the Loan Closing Date), the Company entered into the Loan Agreement with the Lenders for growth capital
loans in an aggregate principal amount of up to $20,000,000 (the Loan), with (i) $15,000,000 funded on the Loan Closing
Date (Tranche 1) and (ii) up to $5,000,000 to be made available to the Company on or prior to September 15, 2022, subject
to the Companys achievement of certain milestones with respect to certain of its ongoing clinical trials. The Loan bears interest
at an annual rate equal to the greater of (a) the sum of 7.00% plus the prime rate as reported in The Wall Street Journal and (b) 10.75%.
The Loan is secured by a lien upon and security interest in all of the Companys assets, including intellectual property, subject
to agreed exceptions. The maturity date of the Loan is December 1, 2024. Up to $5,000,000 of the principal amount of the Loan outstanding
may be converted, at the option of the Lenders, into shares of the Companys Class A common stock at a conversion price of $6.98
per share.
In
connection with the Loan, pursuant to the funding of Tranche 1 on the Loan Closing Date, the Company issued 361,002 Lender Warrants.
The Lender Warrants, which are exercisable until November 30, 2026, were offered and sold by the Company in reliance on the exemption
from registration provided by Section 4(a)(2) of the Securities Act.
On March 31, 2023, the Company filed a Registration Statement on Form S-3 (File No. 333-271054), that was declared effective by the SEC
on April 10, 2023, which related in part to the offer and resale, from time to time, by the Selling Stockholders of up to 50,000 shares
of Class A common stock issuable upon exercise of the Lender Warrants.
The
Lenders may exercise the Lender Warrants at any time, or from time to time up to and including the Expiration Date, by making a cash
payment equal to the exercise price multiplied by the quantity of shares. The Lenders may also exercise the Lender Warrants on a cashless
or net issuance basis by receiving a net number of shares calculated pursuant to the formula set forth in the Lender Warrants.
The Lender Warrants are subject to anti-dilution adjustments for stock dividends, stock splits, and reverse stock splits. Pursuant to
the terms of the Lender Warrants, the holders of the Lender Warrants are entitled to piggyback registration rights if the Company proposes
to file a new registration statement under the Securities Act for purposes of effecting an underwritten offering of its equity securities,
subject to certain limitations.
Use
of Proceeds
Except
as described in any applicable prospectus supplement or in any free writing prospectuses we have authorized for use in connection with
a specific offering, we currently intend to use the net proceeds from the sale of the securities offered by us hereunder, if any, for
working capital and general corporate purposes. We will set forth in the applicable prospectus supplement or free writing prospectus
our intended use for the net proceeds received from the sale of any securities sold pursuant to the prospectus supplement or free writing
prospectus. All of the securities offered by the Selling Securityholders pursuant to this prospectus will be sold by the Selling Securityholders
for their respective accounts. We will not receive any of the proceeds from these sales.
Nasdaq
Listing
Our
Class A common stock is listed on the Nasdaq Capital Market under the symbol BIVI.
Corporate Information
Our
principal executive office is located at 680 W. Nye Lane, Suite 201, Carson City, Nevada 89703, and our phone number is (775) 888-3162.
Our website address is http://www.bioviepharma.com/. The inclusion of our website address does not include or incorporate by reference
into this prospectus supplement or the accompanying prospectus any information on, or accessible through, our website. Our Annual Reports
on Form 10-K, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K, together with amendments to these reports,
are available on the Investor Relations section of our website, free of charge, as soon as reasonably practicable after such
material is electronically filed with, or furnished to, the SEC.
RISK
FACTORS
Investing
in our securities involves risk. The prospectus supplement applicable to a particular offering of securities will contain a discussion
of the risks applicable to an investment in BioVie and to the particular types of securities that we are offering under that prospectus
supplement. Before making an investment decision, you should carefully consider the risks described under Risk Factors
in the applicable prospectus supplement together with all of the other information contained or incorporated by reference in the prospectus
supplement or appearing or incorporated by reference in this prospectus. You should also consider the risks, uncertainties and assumptions
discussed under Part I—Item 1A—Risk Factors of our most recent Annual Report on Form 10-K
and in Part II—Item 1A—Risk Factors in our most recent Quarterly Report on Form 10-Q filed
subsequent to such Form 10-K that are incorporated herein by reference, as may be amended, supplemented or superseded from time
to time by other reports we file with the SEC in the future. Our business, financial condition or results of operations could be materially
adversely affected by any of these risks. The trading price of our securities could decline due to any of these risks, and you may lose
all or part of your investment.
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
This
prospectus, each prospectus supplement and the documents incorporated by reference into this prospectus and each prospectus supplement
contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended, that relate to future events or our future financial performance and involve
known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements
to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking
statements. Such forward-looking statements concern our anticipated results and progress of our operations in future periods, planned
exploration and, if warranted, development of our properties, plans related to our business and other matters that may occur in the future.
These statements relate to analyses and other information that are based on forecasts of future results, estimates of amounts not yet
determinable and assumptions of management. All statements contained herein that are not clearly historical in nature are forward-looking,
and the words anticipate, believe, expect, estimate, may, will,
could, leading, intend, contemplate, shall and similar expressions
are generally intended to identify forward-looking statements. Forward-looking statements are subject to a variety of known and unknown
risks, uncertainties and other factors which could cause actual events or results to differ from those expressed or implied by the forward-looking
statements. The section in this prospectus entitled Risk Factors and the sections in our periodic reports, including
the section in the 2023 Form 10-K entitled Business, and the section in the 2023 Form 10-K and any future Quarterly
Report on Form 10-Qs incorporated herein by reference entitled Managements Discussion and Analysis of Financial Condition
and Results of Operations, as well as other sections in this prospectus and the documents or reports incorporated by reference
into this prospectus, discuss some of the factors that could contribute to these differences. Forward-looking statements in this prospectus,
each prospectus supplement, and the documents incorporated by reference herein and therein include, but are not limited to, statements
with respect to:
| ● | our
limited operating history and experience in developing and manufacturing drugs; |
| ● | none
of our products are approved for commercial sale; |
| ● | our
substantial capital needs; |
| ● | product
development risks; |
| ● | our
lack of sales and marketing personnel; |
| ● | regulatory,
competitive and contractual risks; |
| ● | no
assurance that our product candidates will obtain regulatory approval or that the results
of clinical studies will be favorable; |
| ● | risks
related to our intellectual property rights; |
| ● | the
volatility of the market price and trading volume in our common stock; |
| ● | the
absence of liquidity in our common stock; |
| ● | the
risk of substantial dilution from future issuances of our equity securities; and |
| ● | the
other risks set forth herein and in the documents incorporated by reference herein under
the caption Risk Factors. |
The
foregoing does not represent an exhaustive list of matters that may be covered by the forward-looking statements contained herein or
risk factors that we are faced with. The factors set forth above under Risk Factors and other cautionary statements
made in this prospectus should be read and understood as being applicable to all related forward-looking statements wherever they appear
in this prospectus. The forward-looking statements contained in this prospectus represent our judgment as of the date of this prospectus.
We caution readers not to place undue reliance on such statements. You should read this prospectus and the documents that we have filed
as exhibits to this prospectus and incorporated by reference herein completely and with the understanding that our actual future results
may be materially different from the plans, intentions and expectations disclosed in the forward-looking statements we make. Except as
required by law, we undertake no obligation to update publicly any forward-looking statements for any reason, even if new information
becomes available or other events occur in the future. All subsequent written and oral forward-looking statements attributable to us
or persons acting on our behalf are expressly qualified in their entirety by the cautionary statements contained above and throughout
this prospectus.
This
prospectus and the documents incorporated by reference in this prospectus may contain market data that we obtain from industry sources.
These sources do not guarantee the accuracy or completeness of the information. Although we believe that our industry sources are reliable,
we do not independently verify the information. The market data may include projections that are based on a number of other projections.
While we believe these assumptions to be reasonable and sound as of the date of this prospectus, actual results may differ from the projections.
DIVIDEND
POLICY
We
have never declared or paid dividends on our common stock and we do not anticipate paying any cash dividends on our common stock in the
foreseeable future. Payment of cash dividends, if any, in the future will be at the discretion of our board of directors and will depend
on applicable law and then-existing conditions, including our financial condition, operating results, contractual restrictions, capital
requirements, business prospects and other factors our board of directors may deem relevant. We currently intend to retain all available
funds and any future earnings to fund the development and growth of our business.
USE
OF PROCEEDS
Except
as otherwise provided in the applicable prospectus supplement, we intend to use the net proceeds from the sale of the securities covered
by this prospectus for general corporate purposes, which may include, but is not limited to, working capital, capital expenditures, research
and development expenditures and acquisitions of new technologies or businesses. The precise amount, use and timing of the application
of such proceeds will depend upon our funding requirements and the availability and cost of other capital. Additional information on
the use of net proceeds from an offering of securities covered by this prospectus may be set forth in the prospectus supplement relating
to the specific offering.
We
will not receive any proceeds from the sales of Shares by the Selling Stockholders.
Upon
any exercise of the Lender Warrants by payment of cash, we will receive the cash exercise price paid by the holders of the Lender Warrants.
We cannot assure you that any of the Lender Warrants will be exercised, or if exercised, of the quantity that will be exercised or the
period in which such Lender Warrants will be exercised.
DESCRIPTION
OF CAPITAL STOCK
The
following sections constitute a summary as of the date of this prospectus and do not purport to be a complete description of our capital
stock. We will describe in the applicable prospectus supplement relating to a particular offering the specific terms of the securities
offered by that prospectus supplement. We will indicate in the applicable prospectus supplement if the terms of the securities differ
from the terms we have summarized below. We will also include in the prospectus supplement information, where applicable, material United
States federal income tax considerations relating to the securities.
General
The
following description of common stock of the Company (the common stock) and preferred stock of the Company (the preferred
stock), together with the additional information we include in any applicable prospectus supplement, summarizes the material terms
and provisions of the common stock and preferred stock that we may offer under this prospectus but is not complete. For the complete
terms of our common stock and preferred stock, please refer to our articles of incorporation, as may be amended from time to time (the
Articles of Incorporation), any certificates of designation for our preferred stock, that may be authorized from time to
time, and our amended and restated bylaws, as amended from time to time (the Bylaws). The Nevada General Corporation Law
may also affect the terms of these securities. While the terms we have summarized below will apply generally to any future common stock
or preferred stock that we may offer, we will describe the specific terms of any series of these securities in more detail in the applicable
prospectus supplement. If we so indicate in a prospectus supplement, the terms of any common stock or preferred stock we offer under
that prospectus supplement may differ from the terms we describe below.
As
of August 17, 2023, our authorized capital stock consists of 800,000,000 shares of Class A common
stock, par value $0.0001 per share (the “Class A common stock”), of which 36,826,648 shares of Common Stock were issued, and
36,803,768 shares were issued and outstanding; and 10,000,000 shares of preferred stock, par value $0.001 per share, none of which were
issued and outstanding. The authorized and unissued shares of Class A common stock and preferred stock are available for issuance without
further action by our stockholders, unless such action is required by applicable law or the rules of any stock exchange on which our securities
may be listed. Unless approval of our stockholders is so required, our board of directors will not seek stockholder approval for the issuance
and sale of our common stock.
Class
A Common Stock
Each
holder of Class A common stock is entitled to one vote for each share of Class A common stock held on all matters submitted to a vote
of the stockholders, including the election of directors. Our Articles of Incorporation and Bylaws do not provide for cumulative voting
rights. Subject to preferences that may be applicable to any then outstanding preferred stock, the holders of our outstanding shares
of Class A common stock are entitled to receive dividends, if any, as may be declared from time to time by our board of directors out
of legally available funds. In the event of our liquidation, dissolution or winding up, holders of Class A common stock will be entitled
to share ratably in the net assets legally available for distribution to stockholders after the payment of all of our debts and other
liabilities, subject to the satisfaction of any liquidation preference granted to the holders of any outstanding shares of preferred
stock. Holders of our Class A common stock have no preemptive, conversion or subscription rights, and there are no redemption or sinking
fund provisions applicable to the Class A common stock. The rights, preferences and privileges of the holders of Class A common stock
are subject to, and may be adversely affected by, the rights of the holders of shares of any series of our preferred stock that we may
designate and issue in the future. All of our outstanding shares of Class A common stock are fully paid and nonassessable.
Our
Class A common stock is listed on the Nasdaq Capital Market under the symbol BIVI. The transfer agent and registrar for
our Class A common stock is West Coast Stock Transfer, Inc., Encinitas, California.
Options/Warrants/ Restricted Stock Units
As of August 17, 2023, we had outstanding
options to purchase 3,952,864 shares of our Class A common stock at a weighted average exercise price of $7.10 and outstanding
warrants to purchase 7,770,285 shares of our Class A common stock at a weighted exercise price of $2.06 and restricted stock units
totaling 557,727.
Anti-Takeover
Effects of Our Articles of Incorporation and Bylaws
Our
Articles of Incorporation and Bylaws contain certain provisions that may have anti-takeover effects, making it more difficult for or
preventing a third party from acquiring control of us or changing our Board of Directors and management. According to our Articles of
Incorporation and Bylaws, neither the holders of our common stock nor the holders of any preferred stock we may issue in the future have
cumulative voting rights in the election of our directors. The combination of the present ownership by a few stockholders of a significant
portion of our issued and outstanding common stock and lack of cumulative voting makes it more difficult for other stockholders to replace
our Board of Directors or for a third party to obtain control of us by replacing our Board of Directors.
Anti-Takeover
Effects of Nevada Law
Business
Combinations
The
business combination provisions of Sections 78.411 to 78.444, inclusive, of the Nevada Revised Statutes (NRS)
generally prohibit a Nevada corporation with at least 200 stockholders from engaging in various combination transactions
with any interested stockholder for a period of two years after the date of the transaction in which the person became an interested
stockholder, unless the transaction is approved by the board of directors prior to the date the interested stockholder obtained such
status or the combination is approved by the board of directors and thereafter is approved at a meeting of the stockholders by the affirmative
vote of stockholders representing at least 60% of the outstanding voting power held by disinterested stockholders, and extends beyond
the expiration of the two-year period, unless:
|
● |
the
combination was approved by the board of directors prior to the person
becoming an interested stockholder or the transaction by which the person first became an interested stockholder was approved by the board
of directors before the person became an interested stockholder or the combination is later approved by a majority of the voting power
held by disinterested stockholders; or |
|
● |
if
the consideration to be paid by the interested stockholder is at least equal
to the highest of: (a) the highest price per share paid by the interested stockholder within the two years immediately preceding the date
of the announcement of the combination or in the transaction in which it became an interested stockholder, whichever is higher, (b) the
market value per share of common stock on the date of announcement of the combination and the date the interested stockholder acquired
the shares, whichever is higher, or (c) for holders of preferred stock, the highest liquidation value of the preferred stock, if it is
higher. |
A
combination is generally defined to include mergers or consolidations or any sale, lease exchange, mortgage, pledge, transfer,
or other disposition, in one transaction or a series of transactions, with an interested stockholder having: (a) an aggregate
market value equal to 5% or more of the aggregate market value of the assets of the corporation, (b) an aggregate market value equal
to 5% or more of the aggregate market value of all outstanding shares of the corporation, (c) 10% or more of the earning power or net
income of the corporation, and (d) certain other transactions with an interested stockholder or an affiliate or associate of an interested
stockholder.
In
general, an interested stockholder is a person who, together with affiliates and associates, owns (or within two years,
did own) 10% or more of a corporations voting stock. The statute could prohibit or delay mergers or other takeover or change in
control attempts and, accordingly, may discourage attempts to acquire our Company even though such a transaction may offer our stockholders
the opportunity to sell their stock at a price above the prevailing market price.
Control
Share Acquisitions
The
control share provisions of Sections 78.378 to 78.3793, inclusive, of the NRS apply to issuing corporations
that are Nevada corporations with at least 200 stockholders, including at least 100 stockholders of record who are Nevada residents,
and that conduct business directly or indirectly in Nevada. The control share statute prohibits an acquirer, under certain circumstances,
from voting its shares of a target corporations stock after crossing certain ownership threshold percentages, unless the acquirer
obtains approval of the target corporations disinterested stockholders. The statute specifies three thresholds: one-fifth or more
but less than one-third, one-third but less than a majority, and a majority or more, of the outstanding voting power. Generally, once
an acquirer crosses one of the above thresholds, those shares in an offer or acquisition and acquired within 90 days thereof become control
shares and such control shares are deprived of the right to vote until disinterested stockholders restore the right. These provisions
also provide that if control shares are accorded full voting rights and the acquiring person has acquired a majority or more of all voting
power, all other stockholders who do not vote in favor of authorizing voting rights to the control shares are entitled to demand payment
for the fair value of their shares in accordance with statutory procedures established for dissenters rights.
A
corporation may elect to not be governed by, or opt out of, the control share provisions by making an election in its articles
of incorporation or bylaws, provided that the opt-out election must be in place on the 10th day following the date an acquiring person
has acquired a controlling interest, that is, crossing any of the three thresholds described above. We have not opted out of the control
share statutes, and will be subject to these statutes if we are an issuing corporation as defined in such statutes.
The
effect of the Nevada control share statutes is that the acquiring person, and those acting in association with the acquiring person,
will obtain only such voting rights in the control shares as are conferred by a resolution of the stockholders at an annual or special
meeting. The Nevada control share law, if applicable, could have the effect of discouraging takeovers of our Company.
DESCRIPTION
OF WARRANTS
The
following description, together with the additional information we may include in any applicable prospectus supplements, summarizes the
material terms and provisions of the warrants that we may offer under this prospectus and the related warrant agreements and warrant
certificates. For the avoidance of doubt, this section relates only to new warrants that we may issue and not any of our outstanding
warrants, such as the Lender Warrants, and we refer to such new warrants in this prospectus for the sake of simplicity as warrants.
While
the terms summarized below will apply generally to any warrants that we may offer, we will describe the particular terms of any series
of warrants in more detail in the applicable prospectus supplement. If we indicate in the prospectus supplement, the terms of any warrants
offered under that prospectus supplement may differ from the terms described below. Specific warrant agreements will contain additional
important terms and provisions and will be incorporated by reference as an exhibit to the registration statement, which includes this
prospectus.
General
We
may issue warrants for the purchase of Class A common stock, preferred stock or debt securities, in one or more series. We may issue
warrants independently or together with Class A common stock, preferred stock and/or debt securities, and the warrants may be attached
to or separate from these securities.
We
plan to evidence each series of warrants by warrant certificates that we will issue under a separate warrant agreement. We will enter
into the warrant agreement with a warrant agent. We will indicate the name and address of the warrant agent in the applicable prospectus
supplement relating to a particular series of warrants.
We
will describe in the applicable prospectus supplement the terms of the series of warrants, including:
| ● | the
offering price and aggregate number of warrants offered; |
| ● | the
currency for which the warrants may be purchased; |
| ● | if
applicable, the designation and terms of the securities with which the warrants are issued
and the number of warrants issued with each such security or each principal amount of such
security; |
| ● | if
applicable, the date on and after which the warrants and the related securities will be separately
transferable; |
| ● | the
number of shares of Class A common stock purchasable upon the exercise of one warrant and
the price at which these shares may be purchased upon such exercise; |
| ● | the
effect of any merger, consolidation, sale or other disposition of our business on the warrant
agreement and the warrants; |
| ● | the
terms of any rights to redeem or call the warrants; |
| ● | any
provisions for changes to or adjustments in the exercise price or number of securities issuable
upon exercise of the warrants; |
| ● | the
periods during which, and places at which, the warrants are exercisable; |
| ● | the
dates on which the right to exercise the warrants will commence and expire; |
| ● | the
manner in which the warrant agreement and warrants may be modified; |
| ● | if
applicable, a discussion of certain material U.S. federal income tax considerations of holding
or exercising the warrants; and |
| ● | any
other specific terms, preferences, rights or limitations of or restrictions on the warrants. |
DESCRIPTION
OF DEBT SECURITIES
The
following description, together with the additional information we include in any applicable prospectus supplements, summarizes the material
terms and provisions of the debt securities that we may offer under this prospectus. While the terms we have summarized below will
generally apply to any future debt securities we may offer under this prospectus, we will describe the particular terms of any debt securities
that we may offer in more detail in the applicable prospectus supplement. The terms of any debt securities we offer under a prospectus
supplement may differ from the terms we describe below. As of the date of this prospectus, we have no outstanding registered
debt securities.
We
will issue senior notes under a senior indenture, which we will enter into with the trustee to be named in the senior indenture. We will issue subordinated notes under a subordinated indenture, which we will enter into with the trustee to be named in the subordinated
indenture. We have filed forms of these documents as exhibits to the registration statement of which this prospectus is a part. We use the term indentures to refer to both the senior indenture and the subordinated indenture.
The
indentures will be qualified under the Trust Indenture Act of 1939, as amended (the Trust Indenture Act). We use
the term debenture trustee to refer to either the senior trustee or the subordinated trustee, as applicable.
The
following summaries of material provisions of the senior notes, the subordinated notes and the indentures are subject to, and qualified
in their entirety by reference to, all the provisions of the indenture applicable to a particular series of debt securities. We
urge you to read the applicable prospectus supplements related to the debt securities that we sell under this prospectus, as well as
the complete indentures that contain the terms of the debt securities. Except as we may otherwise indicate, the terms of the senior
and the subordinated indentures are identical.
General
The
terms of each series of debt securities will be established by or pursuant to a resolution of our board of directors and set forth or
determined in the manner provided in an officers certificate or by a supplemental indenture. Debt securities may be issued in
separate series without limitation as to aggregate principal amount. We may specify a maximum aggregate principal amount for the debt
securities of any series. The particular terms of each series of debt securities will be described in a prospectus supplement relating
to such series, including any pricing supplement. The prospectus supplement will set forth:
| ● | the
principal amount being offered, and, if a series, the total amount authorized and the total
amount outstanding; |
| ● | any
limit on the amount that may be issued; |
| ● | whether
or not we will issue the series of debt securities in global form and, if so, the terms and
who the depositary will be; |
| ● | whether
and under what circumstances, if any, we will pay additional amounts on any debt securities
held by a person who is not a U.S. person for tax purposes, and whether we can redeem the
debt securities if we have to pay such additional amounts; |
| ● | the
annual interest rate, which may be fixed or variable, or the method for determining the rate,
the date interest will begin to accrue, the dates interest will be payable and the regular
record dates for interest payment dates or the method for determining such dates; |
| ● | whether
or not the debt securities will be secured or unsecured, and the terms of any secured debt; |
| ● | the
terms of the subordination of any series of subordinated debt; |
| ● | the
place where payments will be payable; |
| ● | restrictions
on transfer, sale or other assignment, if any; |
| ● | our
right, if any, to defer payment of interest and the maximum length of any such deferral period; |
| ● | the
date, if any, after which, the conditions upon which, and the price at which we may, at our
option, redeem the series of debt securities pursuant to any optional or provisional redemption
provisions, and any other applicable terms of those redemption provisions; |
| ● | the
date, if any, on which, and the price at which we are obligated, pursuant to any mandatory
sinking fund or analogous fund provisions or otherwise, to redeem, or at the holders
option to purchase, the series of debt securities and the currency or currency unit in which
the debt securities are payable; |
| ● | whether
the indenture will restrict our ability and/or the ability of our subsidiaries to, among
other things: |
| ● | incur
additional indebtedness; |
| ● | issue
additional securities; |
| ● | pay
dividends and make distributions in respect of our capital stock and the capital stock of
our subsidiaries; |
| ● | place
restrictions on our subsidiaries ability to pay dividends, make distributions or transfer
assets; |
| ● | make
investments or other restricted payments; |
| ● | sell
or otherwise dispose of assets; |
| ● | enter
into sale-leaseback transactions; |
| ● | engage
in transactions with stockholders and affiliates; |
| ● | issue
or sell stock of our subsidiaries; or |
| ● | effect
a consolidation or merger; |
| ● | whether
the indenture will require us to maintain any interest coverage, fixed charge, cash flow-based,
asset-based or other financial ratios; |
| ● | a
discussion of any material or special U.S. federal income tax considerations applicable to
the debt securities; |
| ● | information
describing any book-entry features; |
| ● | provisions
for a sinking fund purchase or other analogous fund, if any; |
| ● | whether
the debt securities are to be offered at a price such that they will be deemed to be offered
at an original issue discount as defined in paragraph (a) of Section 1273 of
the Internal Revenue Code; |
| ● | the
procedures for any auction and remarketing, if any; |
| ● | the
denominations in which we will issue the series of debt securities, if other than denominations
of $1,000 and any integral multiple thereof; |
| ● | if
other than dollars, the currency in which the series of debt securities will be denominated;
and |
| ● | any
other specific terms, preferences, rights or limitations of, or restrictions on, the debt
securities, including any events of default that are in addition to those described in this
prospectus or any covenants provided with respect to the debt securities that are in addition
to those described above, and any terms that may be required by us or advisable under applicable
laws or regulations or advisable in connection with the marketing of the debt securities. |
Conversion
or Exchange Rights
We
will set forth in the prospectus supplement the terms on which a series of debt securities may be convertible into or exchangeable for
Class A common stock or other securities of ours or a third party, including the conversion or exchange rate, as applicable, or how it
will be calculated, and the applicable conversion or exchange period. We will include provisions as to whether conversion or exchange
is mandatory, at the option of the holder or at our option. We may include provisions pursuant to which the number of our securities
or the securities of a third party that the holders of the series of debt securities receive upon conversion or exchange would, under
the circumstances described in those provisions, be subject to adjustment, or pursuant to which those holders would, under those circumstances,
receive other property upon conversion or exchange, for example in the event of our merger or consolidation with another entity.
Consolidation,
Merger or Sale
The
indentures in the forms initially filed as exhibits to the registration statement of which this prospectus is a part do not contain
any covenant that restricts our ability to merge or consolidate, or sell, convey, transfer or otherwise dispose of all or
substantially all of our assets. However, any successor of ours or the acquirer of such assets must assume all of our obligations
under the indentures and the debt securities. If the debt securities are convertible for our other securities, the person
with whom we consolidate or merge or to whom we sell all of our property must make provisions for the conversion of the debt
securities into securities that the holders of the debt securities would have received if they had converted the debt securities
before the consolidation, merger or sale.
Events
of Default Under the Indenture
The
following are events of default under the indentures in the forms initially filed as exhibits to the registration statement with respect
to any series of debt securities that we may issue:
| ● | if
we fail to pay interest when due and payable and our failure continues for 90 days and the
time for payment has not been extended or deferred; |
| ● | if
we fail to pay the principal, sinking fund payment or premium, if any, when due and payable
and the time for payment has not been extended or delayed; |
| ● | if
we fail to observe or perform any other covenant contained in the debt securities or the
indentures, other than a covenant specifically relating to another series of debt securities,
and our failure continues for 90 days after we receive notice from the debenture trustee
or holders of at least 25% in aggregate principal amount of the outstanding debt securities
of the applicable series; and |
| ● | if
specified events of bankruptcy, insolvency or reorganization occur. |
If
an event of default with respect to debt securities of any series occurs and is continuing, other than an event of default specified
in the last bullet point above, the debenture trustee or the holders of at least 25% in aggregate principal amount of the outstanding
debt securities of that series, by notice to us in writing, and to the debenture trustee if notice is given by such holders, may declare
the unpaid principal of, premium, if any, and accrued interest, if any, due and payable immediately. If an event of default specified
in the last bullet point above occurs with respect to us, the principal amount of and accrued interest, if any, of each issue of debt
securities then outstanding shall be due and payable without any notice or other action on the part of the debenture trustee or any holder.
The
holders of a majority in principal amount of the outstanding debt securities of an affected series may waive any default or event of
default with respect to the series and its consequences, except defaults or events of default regarding payment of principal, premium,
if any, or interest, unless we have cured the default or event of default in accordance with the indenture. Any waiver shall cure
the default or event of default.
Subject
to the terms of the indentures, if an event of default under an indenture shall occur and be continuing, the debenture trustee will be
under no obligation to exercise any of its rights or powers under such indenture at the request or direction of any of the holders of
the applicable series of debt securities, unless such holders have offered the debenture trustee reasonable indemnity. The holders
of a majority in principal amount of the outstanding debt securities of any series will have the right to direct the time, method and
place of conducting any proceeding for any remedy available to the debenture trustee, or exercising any trust or power conferred on the
debenture trustee, with respect to the debt securities of that series, provided that:
| ● | the
direction so given by the holder is not in conflict with any law or the applicable indenture;
and |
| ● | subject
to its duties under the Trust Indenture Act, the debenture trustee need not take any action
that might involve it in personal liability or might be unduly prejudicial to the holders
not involved in the proceeding. |
A
holder of the debt securities of any series will only have the right to institute a proceeding under the indentures or to appoint a receiver
or trustee, or to seek other remedies if:
| ● | the
holder has given written notice to the debenture trustee of a continuing event of default
with respect to that series; |
| ● | the
holders of at least 25% in aggregate principal amount of the outstanding debt securities
of that series have made written request, and such holders have offered reasonable indemnity,
to the debenture trustee to institute the proceeding as trustee; and |
| ● | the
debenture trustee does not institute the proceeding and does not receive from the holders
of a majority in aggregate principal amount of the outstanding debt securities of that series
other conflicting directions within 90 days after the notice, request and offer. |
These
limitations do not apply to a suit instituted by a holder of debt securities if we default in the payment of the principal, premium,
if any, or interest on, the debt securities.
We
will periodically file statements with the debenture trustee regarding our compliance with specified covenants in the indentures.
Modification
of Indenture; Waiver
We
and the debenture trustee may change an indenture without the consent of any holders with respect to specific matters, including:
| ● | to
fix any ambiguity, defect or inconsistency in the indenture; |
| ● | to
comply with the provisions described above under Consolidation, Merger or Sale; |
| ● | to
comply with any requirements of the SEC in connection with the qualification of any indenture
under the Trust Indenture Act; |
| ● | to
evidence and provide for the acceptance of appointment hereunder by a successor trustee; |
| ● | to
provide for uncertificated debt securities and to make all appropriate changes for such purpose; |
| ● | to
add to, delete from, or revise the conditions, limitations and restrictions on the authorized
amount, terms or purposes of issuance, authorization and delivery of debt securities or any
series, as set forth in the indenture; |
| ● | to
provide for the issuance of and establish the form and terms and conditions of the debt securities
of any series as provided under General to establish the form of any certifications
required to be furnished pursuant to the terms of the indenture or any series of debt securities,
or to add to the rights of the holders of any series of debt securities; |
| ● | to
add to our covenants such new covenants, restrictions, conditions or provisions for the protection
of the holders, to make the occurrence, or the occurrence and the continuance, of a default
in any such additional covenants, restrictions, conditions or provisions an event of default,
or to surrender any of our rights or powers under the indenture; or |
| ● | to
change anything that does not materially adversely affect the interests of any holder of
debt securities of any series. |
In
addition, under the indentures, the rights of holders of a series of debt securities may be changed by us and the debenture trustee with
the written consent of the holders of at least a majority in aggregate principal amount of the outstanding debt securities of each series
that is affected. However, we and the debenture trustee may only make the following changes with the consent of each holder of
any outstanding debt securities affected:
| ● | extending
the fixed maturity of the series of debt securities; |
| ● | reducing
the principal amount, reducing the rate of or extending the time of payment of interest,
or reducing any premium payable upon the redemption of any debt securities; or |
| ● | reducing
the percentage of debt securities, the holders of which are required to consent to any amendment,
supplement, modification or waiver. |
Discharge
Each
indenture provides that we can elect to be discharged from our obligations with respect to one or more series of debt securities, except
that the following obligations survive until the maturity date or the redemption date:
| ● | register
the transfer or exchange of debt securities of the series; |
| ● | replace
stolen, lost or mutilated debt securities of the series; |
| ● | maintain
paying agencies; |
| ● | hold
monies for payment in trust; and |
| ● | appoint
any successor trustee; |
and
the following obligations survive the maturity date or the redemption date:
| ● | recover
excess money held by the debenture trustee; and |
| ● | compensate
and indemnify the debenture trustee. |
In
order to exercise our rights to be discharged, we must deposit with the debenture trustee money or government obligations sufficient
to pay all the principal of, any premium, if any, and interest on, the debt securities of the series on the dates payments are due.
Form,
Exchange and Transfer
We
will issue the debt securities of each series only in fully registered form without coupons and, unless we otherwise specify in the applicable
prospectus supplement, in denominations of $1,000 and any integral multiple thereof. The indentures provide that we may issue debt
securities of a series in temporary or permanent global form and as book-entry securities that will be deposited with, or on behalf of,
The Depository Trust Company, New York, New York, known as DTC, or another depositary named by us and identified in a prospectus supplement
with respect to that series.
At
the option of the holder, subject to the terms of the indentures and the limitations applicable to global securities described in the
applicable prospectus supplement, the holder of the debt securities of any series can exchange the debt securities for other debt securities
of the same series, in any authorized denomination and of like tenor and aggregate principal amount.
Subject
to the terms of the indentures and the limitations applicable to global securities set forth in the applicable prospectus supplement,
holders of the debt securities may present the debt securities for exchange or for registration of transfer, duly endorsed or with the
form of transfer endorsed thereon duly executed if so required by us or the security registrar, at the office of the security registrar
or at the office of any transfer agent designated by us for this purpose. Unless otherwise provided in the debt securities that
the holder presents for transfer or exchange, we will make no service charge for any registration of transfer or exchange, but we may
require payment of any taxes or other governmental charges.
We
will name in the applicable prospectus supplement the security registrar, and any transfer agent in addition to the security registrar,
that we initially designate for any debt securities. We may at any time designate additional transfer agents or rescind the designation
of any transfer agent or approve a change in the office through which any transfer agent acts, except that we will be required to maintain
a transfer agent in each place of payment for the debt securities of each series.
If
we elect to redeem the debt securities of any series, we will not be required to:
| ● | issue,
register the transfer of, or exchange any debt securities of any series being redeemed in
part during a period beginning at the opening of business 15 days before the day of mailing
of a notice of redemption of any debt securities that may be selected for redemption and
ending at the close of business on the day of the mailing; or |
| ● | register
the transfer of or exchange any debt securities so selected for redemption, in whole or in
part, except the unredeemed portion of any debt securities we are redeeming in part. |
Information
Concerning the Debenture Trustee
The
debenture trustee, other than during the occurrence and continuance of an event of default under an indenture, undertakes to perform
only those duties as are specifically set forth in the applicable indenture. Upon an event of default under an indenture, the debenture
trustee must use the same degree of care as a prudent person would exercise or use in the conduct of his or her own affairs. Subject
to this provision, the debenture trustee is under no obligation to exercise any of the powers given it by the indentures at the request
of any holder of debt securities unless it is offered reasonable security and indemnity against the costs, expenses and liabilities that
it might incur.
Payment
and Paying Agents
Unless
we otherwise indicate in the applicable prospectus supplement, we will make payment of the interest on any debt securities on any interest
payment date to the person in whose name the debt securities, or one or more predecessor securities, are registered at the close of business
on the regular record date for the interest.
We
will pay principal of and any premium and interest on the debt securities of a particular series at the office of the paying agents designated
by us, except that, unless we otherwise indicate in the applicable prospectus supplement, we may make interest payments by check that
we will mail to the holder or by wire transfer to certain holders. Unless we otherwise indicate in a prospectus supplement, we
will designate the corporate office of the debenture trustee in the State of Nevada as our sole paying agent for payments with respect
to debt securities of each series. We will name in the applicable prospectus supplement any other paying agents that we initially
designate for the debt securities of a particular series. We will maintain a paying agent in each place of payment for the debt
securities of a particular series.
All
money we pay to a paying agent or the debenture trustee for the payment of the principal of or any premium or interest on any debt securities
that remains unclaimed at the end of two years after such principal, premium or interest has become due and payable will be repaid to
us, and the holder of the debt security thereafter may look only to us for payment thereof.
Governing
Law
The
indentures and the debt securities will be governed by and construed in accordance with the laws of the State of Nevada, except to the
extent that the Trust Indenture Act is applicable.
Subordination
of Subordinated Debt Securities
The
subordinated debt securities will be subordinate and junior in priority of payment to certain of our other indebtedness to the extent
described in a prospectus supplement. The indentures in the forms initially filed as exhibits to the registration statement of
which this prospectus is a part do not limit the amount of indebtedness that we may incur, including senior indebtedness or subordinated
indebtedness, and do not limit us from issuing any other debt, including secured debt or unsecured debt.
DESCRIPTION
OF RIGHTS
The
complete terms of the rights will be contained in the rights agreements we enter into with rights agents. These documents will be included
or incorporated by reference as exhibits to the registration statement of which this prospectus is a part. You should read the rights
agreements and any related documents. You also should read the prospectus supplement, which will contain additional information and which
may update or change some of the information below.
This
section describes the general terms of the rights to purchase Class A common stock or other securities that we may offer to stockholders
using this prospectus. Further terms of the rights will be stated in the applicable prospectus supplement (or applicable free writing
prospectus). The following description and any description of the rights in a prospectus supplement (or applicable free writing prospectus)
may not be complete and is subject to and qualified in its entirety by reference to the terms of any agreement relating to the rights.
Rights
may be issued independently or together with any other security and may or may not be transferable. As part of any rights offering, we
may enter into a standby underwriting or other arrangement under which the underwriters or any other person would purchase any securities
that are not purchased in such rights offering. If we issue rights, each series of rights will be issued under a separate rights agreement
to be entered into between us and a bank or trust company, as rights agent, that will be named in the applicable prospectus supplement.
Further terms of the rights will be stated in the applicable prospectus supplement. The rights agent will act solely as our agent and
will not assume any obligation to any holders of rights certificates or beneficial owners of rights. The rights agreements and rights
certificates will be filed with the SEC as an exhibit to the registration statement of which this prospectus is a part or as an exhibit
to a filing incorporated by reference in the registration statement. See Where You Can Find Additional Information
for information on how to obtain copies of the rights agreements and rights certificates.
The
prospectus supplement relating to any rights we offer will describe the specific terms of the offering and the rights, including the
record date for stockholders entitled to the rights distribution, the number of rights issued and the number of shares of Class A common
stock that may be purchased upon exercise of the rights, the exercise price of the rights, the date on which the rights will become effective
and the date on which the rights will expire, and any applicable U.S. federal income tax considerations.
In
general, a right entitles the holder to purchase for cash a specific number of shares of Class A common stock or other securities at
a specified exercise price. The rights are normally issued to stockholders as of a specific record date, may be exercised only for a
limited period of time and become void following the expiration of such period. If we determine to issue rights, we will accompany this
prospectus with a prospectus supplement that will describe, among other things:
| ● | the
record date for stockholders entitled to receive the rights; |
| ● | the
number of shares of Class A common stock or other securities that may be purchased upon exercise
of each right; |
| ● | the
exercise price of the rights; |
| ● | the
terms for changes to or adjustments in the exercise price, if any; |
| ● | whether
the rights are transferable; |
| ● | the
period during which the rights may be exercised and when they will expire; |
| ● | the
steps required to exercise the rights; |
| ● | whether
the rights include oversubscription rights so that the holder may purchase
more securities if other holders do not purchase their full allotments; |
| ● | whether
we intend to sell the shares of Class A common stock or other securities that are not purchased
in the rights offering to an underwriter or other purchaser under a contractual standby
commitment or other arrangement; |
| ● | our
ability to withdraw or terminate the rights offering; |
| ● | any
material United States federal income tax consequences; and |
| ● | other
material terms, including terms relating to transferability, exchange, exercise or amendment
of the rights. |
If
fewer than all of the rights issued in any rights offering are exercised, we may offer any unsubscribed securities directly to persons
other than stockholders, to or through agents, underwriters or dealers or through a combination of such methods, including pursuant to
standby arrangements, as described in the applicable prospectus supplement. After the close of business on the expiration date, all unexercised
rights will become void.
DESCRIPTION
OF UNITS
We
may issue units comprised of shares of Class A common stock, shares of preferred stock, debt securities, rights and warrants to purchase
Class A common stock in any combination. We may issue units in such amounts and in as many distinct series as we wish. This section outlines
certain provisions of the units that we may issue. If we issue units, they will be issued under one or more unit agreements to be entered
into between us and a bank or other financial institution, as unit agent. The information described in this section may not be complete
in all respects and is qualified entirely by reference to the unit agreement with respect to the units of any particular series. The
specific terms of any series of units offered will be described in the applicable prospectus supplement. If so described in a particular
supplement, the specific terms of any series of units may differ from the general description of terms presented below. We urge you to
read any prospectus supplement related to any series of units we may offer, as well as the complete unit agreement and unit certificate
that contain the terms of the units. If we issue units, forms of unit agreements and unit certificates relating to such units will be
incorporated by reference as exhibits to the registration statement, which includes this prospectus.
Each
unit that we may issue will be issued so that the holder of the unit is also the holder of each security included in the unit. Thus,
the holder of a unit will have the rights and obligations of a holder of each included security. The unit agreement under which a unit
is issued may provide that the securities included in the unit may not be held or transferred separately, at any time or at any time
before a specified date.
The
applicable prospectus supplement may describe:
| ● | the
designation and terms of the units and of the securities comprising the units, including
whether and under what circumstances those securities may be held or transferred separately; |
| ● | any
provisions of the governing unit agreement; |
| ● | the
price or prices at which such units will be issued; |
| ● | the
applicable U.S. federal income tax considerations relating to the units; |
| ● | any
provisions for the issuance, payment, settlement, transfer or exchange of the units or of
the securities comprising the units; and |
| ● | any
other terms of the units and of the securities comprising the units. |
The
provisions described in this section, as well as those described under Description of Capital Stock, Description
of Debt Securities and Description of Warrants will apply to the securities included in each unit, to
the extent relevant and as may be updated in any prospectus supplements. We may issue units in such amounts and in as many distinct series
as we wish. This section summarizes terms of the units that apply generally to all series. Most of the financial and other specific terms
of a particular series of units will be described in the applicable prospectus supplement.
Unit
Agreements
We
will issue the units under one or more unit agreements to be entered into between us and a bank or other financial institution, as unit
agent. We may add, replace or terminate unit agents from time to time. We will identify the unit agreement under which each series of
units will be issued and the unit agent under that agreement in the applicable prospectus supplement.
The
following provisions will generally apply to all unit agreements unless otherwise stated in the applicable prospectus supplement:
Modification
Without Consent
We
and the applicable unit agent may amend any unit or unit agreement without the consent of any holder:
| ● | to
cure any ambiguity in any provisions of the governing unit agreement that differ from those
described below; |
| ● | to
correct or supplement any defective or inconsistent provision; or |
| ● | to
make any other change that we believe is necessary or desirable and will not adversely affect
the interests of the affected holders in any material respect. |
We
do not need any approval to make changes that affect only units to be issued after the changes take effect. We may also make changes
that do not adversely affect a particular unit in any material respect, even if they adversely affect other units in a material respect.
In those cases, we do not need to obtain the approval of the holder of the unaffected unit; we need only obtain any required approvals
from the holders of the affected units.
Modification
With Consent
We
may not amend any particular unit or a unit agreement with respect to any particular unit unless we obtain the consent of the holder
of that unit, if the amendment would:
| ● | impair
any right of the holder to exercise or enforce any right under a security included in the
unit if the terms of that security require the consent of the holder to any changes that
would impair the exercise or enforcement of that right; or |
| ● | reduce
the percentage of outstanding units or any series or class the consent of whose holders is
required to amend that series or class, or the applicable unit agreement with respect to
that series or class, as described below. |
| | Any other change
to a particular unit agreement and the units issued under that agreement would require the following approval: |
| ● | if
the change affects only the units of a particular series issued under that agreement, the
change must be approved by the holders of a majority of the outstanding units of that series;
or |
| ● | if
the change affects the units of more than one series issued under that agreement, it must
be approved by the holders of a majority of all outstanding units of all series affected
by the change, with the units of all the affected series voting together as one class for
this purpose. |
These
provisions regarding changes with majority approval also apply to changes affecting any securities issued under a unit agreement, as
the governing document.
In
each case, the required approval must be given by written consent.
Unit
Agreements Will Not be Qualified Under Trust Indenture Act
No
unit agreement will be qualified as an indenture, and no unit agent will be required to qualify as a trustee, under the Trust Indenture
Act. Therefore, holders of units issued under unit agreements will not have the protections of the Trust Indenture Act with respect to
their units.
Mergers
and Similar Transactions Permitted; No Restrictive Covenants or Events of Default
The
unit agreements will not restrict our ability to merge or consolidate with, or sell our assets to, another corporation or other entity
or to engage in any other transactions. If at any time we merge or consolidate with, or sell our assets substantially as an entirety
to, another corporation or other entity, the successor entity will succeed to and assume our obligations under the unit agreements. We
will then be relieved of any further obligation under these agreements.
The
unit agreements will not include any restrictions on our ability to put liens on our assets, nor will they restrict our ability to sell
our assets. The unit agreements also will not provide for any events of default or remedies upon the occurrence of any events of default.
Form,
Exchange and Transfer
We
will issue each unit in global (i.e., book-entry) form only. Units in book-entry form will be represented by a global security registered
in the name of a depositary, which will be the holder of all the units represented by the global security. Those who own beneficial interests
in a unit will do so through participants in the depositarys system, and the rights of these indirect owners will be governed
solely by the applicable procedures of the depositary and its participants. We will describe book-entry securities, and other terms regarding
the issuance and registration of the units in the applicable prospectus supplement.
Each
unit and all securities comprising the unit will be issued in the same form.
If
we issue any units in registered, non-global form, the following will apply to them:
| ● | The
units will be issued in the denominations stated in the applicable prospectus supplement.
Holders may exchange their units for units of smaller denominations or combined into fewer
units of larger denominations, as long as the total amount is not changed. |
| ● | Holders
may exchange or transfer their units at the office of the unit agent. Holders may also replace
lost, stolen, destroyed or mutilated units at that office. We may appoint another entity
to perform these functions or perform them ourselves. |
| ● | Holders
will not be required to pay a service charge to transfer or exchange their units, but they
may be required to pay for any tax or other governmental charge associated with the transfer
or exchange. The transfer or exchange, and any replacement, will be made only if our transfer
agent is satisfied with the holders proof of legal ownership. The transfer agent may
also require an indemnity before replacing any units. |
| ● | If
we have the right to redeem, accelerate or settle any units before their maturity, and we
exercise our right as to less than all those units or other securities, we may block the
exchange or transfer of those units during the period beginning 15 days before the day we
mail the notice of exercise and ending on the day of that mailing, in order to freeze the
list of holders to prepare the mailing. We may also refuse to register transfers of or exchange
any unit selected for early settlement, except that we will continue to permit transfers
and exchanges of the unsettled portion of any unit being partially settled. We may also block
the transfer or exchange of any unit in this manner if the unit includes securities that
are or may be selected for early settlement. |
Only
the depositary will be entitled to transfer or exchange a unit in global form, since it will be the sole holder of the unit.
Payments
and Notices
In
making payments and giving notices with respect to our units, we will follow the procedures as described in the applicable prospectus
supplement.
SELLING
STOCKHOLDERS
On
November 30, 2021, we entered into the Loan Agreement pursuant to which we issued and sold to the Selling Stockholders Lender Warrants
to purchase 361,002 shares of Class A common stock. This prospectus covers the sale or other disposition by the Selling Stockholders
and their respective donees, pledgees or other successors-in-interest of up to the total number of Shares registered on behalf of the
Selling Stockholders in the manner contemplated under Plan of Distribution below. Throughout this prospectus, when
we refer to the Shares being registered on behalf of the Selling Stockholders, we are referring to the Shares issuable upon the exercise
of the Lender Warrants issued to the Selling Stockholders in the Loan, and when we refer to the Selling Stockholders in this prospectus,
we are referring to those investors set forth in the table below.
On
March 31, 2023, the Company filed a Registration Statement on Form S-3 (File No. 333-271054), that was declared effective by the SEC
on April 10, 2023, which related in part to the offer and resale, from time to time, by the Selling Stockholders of up to 50,000 shares
of Class A common stock issuable upon exercise of the Lender Warrants.
In
connection with the Loan Agreement, we granted certain registration rights to the Selling Stockholders. The Loan Agreement also provide,
among other things, certain indemnification rights and reimbursement by the Company of certain fees and expenses.
We
have agreed with the Selling Stockholders to keep the registration statement of which this prospectus constitutes a part effective for
a period of at least twelve (12) months after the date that the Selling Stockholders are first given the opportunity to sell all of the
Shares.
Except
as otherwise disclosed herein and in the footnotes below with respect to the Selling Stockholders, the Selling Stockholders do not, and
within the past three years, have not had, any position, office or other material relationship with us.
The
following table sets forth the name of the Selling Stockholders, the number of shares of Class A common stock beneficially owned by the
Selling Stockholders, the number of Shares that may be offered under this prospectus and the number of shares of our Class A common stock
that will be owned by the Selling Stockholders assuming all of the Shares covered hereby are sold. The number of Shares in the column
Number of Shares Being Offered represents all of the Shares that the Selling Stockholders may offer under this prospectus.
Pursuant to Rules 13d-3 and 13d-5 of the Exchange Act (Rule 13(d)), beneficial ownership includes all shares of our Class
A common stock as to which a Selling Stockholder has sole or shared voting power or investment power, and also any shares of our Class
A common stock which the Selling Stockholder has the right to acquire within 60 days of August 17, 2023, but without regard to the
Beneficial Ownership Limitation included in the Lender Warrants (described below). The actual beneficial ownership of certain Selling
Stockholders (determined in accordance with Rule 13d) does not necessarily correspond to the number of Shares reflected below in the
column Number of Shares Being Offered.
Notwithstanding
the presentation of Share ownership in the table below, pursuant to the terms of the Lender Warrants, a holder of a Lender Warrant does
not have the right to exercise any portion of the Lender Warrant held by such holder to the extent (but only to the extent) that after
giving effect to such issuance after exercise, the holder (together with the holders affiliates, and any other persons acting
as a group together with the holder or any of the holders affiliates), would beneficially own in excess of 9.99% of the number
of shares of Class A common stock outstanding immediately after giving effect to the issuance of shares of Class A common stock issued
upon exercise of the Lender Warrants (the Beneficial Ownership Limitation). The holder of a Lender Warrant may, upon notice
to the Company, increase or decrease the Beneficial Ownership Limitation of its Warrant, provided that the Beneficial Ownership Limitation
in no event exceeds 9.99% of the number of shares of the Class A common stock outstanding immediately after giving effect to the issuance
of shares of Class A common stock upon exercise of the Lender Warrant held by the holder. Any increase in the Beneficial Ownership Limitation
will not be effective until the 61st day after such notice is delivered to the Company. No such increase notice has been provided
to the Company as of the date of this prospectus.
The information set forth below is based upon information
obtained from the Selling Stockholders and upon information in our possession regarding the issuance of the Shares issuable upon the exercise
of the Lender Warrants to the Selling Stockholders. The percentages of shares of Class A common stock beneficially owned before this offering
are based on 36,803,768 shares of Class A common stock issued and outstanding as of August 17, 2023. The percentages of shares of our
Class A common stock owned after the offering are based on 37,114,770 shares of our Class A common stock outstanding after this offering,
including the 36,803,768 shares of Class A common stock outstanding as of August 17, 2023 plus 311,002 Shares issuable upon the exercise
of the Lender Warrants covered hereby.
The
Shares covered hereby may be offered from time to time by the Selling Stockholders. The Selling Stockholders may sell some, all or none
of their respective Shares. We do not know how long the Selling Stockholders will hold their Shares before selling them, and we currently
have no agreements, arrangements or understandings with the Selling Stockholders regarding the sale or other disposition of any of the
Shares
|
|
Shares
of Class A common stock
Beneficially Owned
Prior To The
Offering |
|
|
Maximum
Number of
Shares
Being Offered |
|
|
Shares
of Class A common stock
Beneficially Owned
After The
Offering(1) |
|
Name
of Selling Stockholder |
|
Number |
|
Percentage |
|
|
Number |
|
|
Percent |
|
Avenue
Venture Opportunities Fund, LP(2) |
|
155,501 |
|
* |
|
|
155,501 |
|
|
0 |
|
|
- |
|
Avenue
Venture Opportunities Fund II, LP(3) |
|
155,501 |
|
* |
|
|
155,501 |
|
|
0 |
|
|
- |
|
Percentages
denoted by * are less than 1%.
| (1) | Assumes
that all Shares being registered in this prospectus are resold to third parties and that
the Selling Stockholders sell all Shares registered under this prospectus held by them. |
| (2) | The
business address for Avenue Venture Opportunities Fund, LP is 11 West 42nd St. 9th Floor,
New York, NY, 10036. |
| (3) | The
business address for Avenue Venture Opportunities Fund II, LP is 11 West 42nd St. 9th Floor,
New York, NY, 10036. |
PLAN
OF DISTRIBUTION
We
may sell the securities described herein, and the Selling Stockholders may sell some or all of the Shares that they hold, from time to
time in one or more offerings, by a variety of methods, including the following:
| ● | on
any national securities exchange or quotation service on which our securities may be listed
at the time of sale, including the Nasdaq Capital Market; |
| ● | in
the over-the-counter market; |
| ● | in
transactions otherwise than on such exchange or in the over-the-counter market, which may
include privately negotiated transactions and sales directly to one or more purchasers; |
| ● | through
one or more agents, including an at the market offering within the meaning
of Rule 415(a)(4) under the Securities Act; |
| ● | through
ordinary brokerage transactions and transactions in which the broker-dealer solicits purchasers; |
| ● | through
purchases by a broker-dealer as principal and resale by the broker-dealer for its account; |
| ● | to
or through underwriters, broker-dealers, agents, in privately negotiated transactions, or
any combination of these methods; |
| ● | through
the writing or settlement of options or other hedging transactions, whether through an options
exchange or otherwise; |
| ● | by
pledge to secure debts or other obligations; |
| ● | block
trades in which the broker-dealer so engaged will attempt to sell the securities as agent
but may position and resell a portion of the block as principal to facilitate the transaction,
or crosses in which the same broker acts as agent on both sides of the trade; |
| ● | a
combination of any of these methods; or |
| ● | by
any other method permitted pursuant to applicable law. |
As
used in this prospectus, Selling Stockholders includes transferees, pledgees, donees, assignees or successors selling shares
received after the date of this prospectus from a Selling Stockholder as a gift, pledge, partnership distribution or other non-sale related
transfer.
We
will not receive any proceeds from the sale of securities that may be sold from time to time pursuant to this prospectus by the Selling
Stockholders. We will bear the costs associated with this registration in accordance with the agreements granting registration rights
to the Selling Stockholders. However, the Selling Stockholders will bear any brokerage commissions, transfer taxes, or underwriting commissions
and discounts attributable to their sale of securities pursuant to this prospectus. To our knowledge, there are currently no plans, arrangements
or understandings between any Selling Stockholders and any underwriter, broker-dealer or agent regarding the sale of securities pursuant
to this prospectus by the Selling Stockholders.
We
or the Selling Stockholders may sell the securities to or through one or more underwriters or dealers (acting as principal or agent),
through agents, or directly to one or more purchasers. We or the Selling Stockholders may distribute the securities from time to time
in one or more transactions:
| ● | at
a fixed price or prices, which may be changed; |
| ● | at
market prices prevailing at the time of sale; |
| ● | at
prices related to such prevailing market prices; |
| ● | at
varying prices determined at the time of sale; or |
We
will describe the terms of the offering of the securities and the specific plan of distribution in a prospectus supplement or supplements
to this prospectus, any related free writing prospectus that we may authorize to be provided to you, an amendment to the registration
statement of which this prospectus is a part or other filings we make with the SEC under the Exchange Act that are incorporated by reference.
Such description may include, to the extent applicable:
| ● | the
name or names of any underwriters, dealers, agents or other purchasers; |
| ● | the
purchase price of the securities or other consideration therefor, and the proceeds, if any,
we or the Selling Stockholders will receive from the sale; |
| ● | any
options to purchase additional shares or other options under which underwriters, dealers,
agents or other purchasers may purchase additional securities from us or the Selling Stockholders; |
| ● | any
agency fees or underwriting discounts and other items constituting agents or underwriters
compensation; |
| ● | any
public offering price; |
| ● | any
discounts or concessions allowed or reallowed or paid to dealers; and |
| ● | any
securities exchange or market on which the securities may be listed. |
Only
underwriters named in the prospectus supplement will be underwriters of the securities offered by the prospectus supplement. The Selling
Stockholders who participate in the sale or distribution of the securities offered by the Selling Stockholders and any dealers and agents
participating in the distribution of the securities may be deemed to be underwriters, and compensation received by them on resale of
the securities may be deemed to be underwriting discounts. Any Selling Stockholders identified as registered broker-dealers in the Selling
Stockholders table in the section titled Selling Stockholders are deemed to be underwriters. If such dealers or
agents were deemed to be underwriters, they may be subject to statutory liabilities under the Securities Act.
If
underwriters are used in the sale, they will acquire the securities for their own account and may resell the securities from time to
time in one or more transactions at a fixed public offering price or at varying prices determined at the time of sale. The obligations
of the underwriters to purchase the securities will be subject to the conditions set forth in the applicable underwriting agreement.
We or the Selling Stockholders may offer the securities to the public through underwriting syndicates represented by managing underwriters
or by underwriters without a syndicate. Subject to certain conditions, the underwriters will be obligated to purchase all of the securities
offered by the prospectus supplement, other than securities covered by any option to purchase additional shares or other option. If a
dealer is used in the sale of securities, we or the Selling Stockholders, or an underwriter, will sell the securities to the dealer,
as principal. The dealer may then resell the securities to the public at varying prices to be determined by the dealer at the time of
resale. To the extent required, we will set forth in the prospectus supplement the name of the dealer and the terms of the transaction.
Any public offering price and any discounts or concessions allowed or reallowed or paid to dealers may change from time to time. We or
the Selling Stockholders may use underwriters, dealers or agents with whom we have a material relationship. We will describe in the prospectus
supplement, naming the underwriter, dealer or agent, the nature of any such relationship.
We
or the Selling Stockholders may sell securities directly or through agents we designate from time to time. If required by applicable
law, we will name any agent involved in the offering and sale of securities and we will describe any commissions payable to the agent
in the prospectus supplement. Unless the prospectus supplement states otherwise, the agent will act on a best-efforts basis for the period
of its appointment.
We
may provide agents, dealers and underwriters with indemnification against civil liabilities, including liabilities under the Securities
Act, or contribution with respect to payments that the agents or dealers or underwriters may make with respect to these liabilities.
Agents, dealers and underwriters or their affiliates may engage in transactions with, or perform services for us in the ordinary course
of business.
With
respect to the offering and sale of securities under this prospectus by the Selling Stockholders, we have agreed to indemnify each Selling
Stockholder and any underwriter for such Selling Stockholder (as determined in the Securities Act) against specified liabilities, including
liabilities under the Securities Act. The Selling Stockholders have agreed to indemnify us against specified liabilities, including liabilities
under the Securities Act. In addition, we have agreed to pay substantially all of the expenses incidental to the registration, offering
and sale of securities pursuant to this prospectus by the Selling Stockholders to the public, including the payment of federal securities
law and state blue sky registration fees and the reasonable fees and disbursements of one counsel for the Selling Stockholders, except
that we will not bear any brokers or underwriters discounts and commissions, fees and expenses of counsel to underwriters
or brokers, transfer taxes or transfer fees relating to the sale of securities by the Selling Stockholders.
We
may engage in at-the-market offerings into an existing trading market in accordance with rule 415(a)(4) under the Securities Act. In
addition, we or the Selling Stockholders may enter into derivative transactions with third parties, or sell securities not covered by
this prospectus to third parties in privately negotiated transactions. If the applicable prospectus supplement so indicates, in connection
with those derivatives, the third parties may sell securities covered by this prospectus and the applicable prospectus supplement, including
in short sale transactions. If so, the third party may use securities pledged by us or the Selling Stockholders or borrowed from us,
the Selling Stockholders or others to settle those sales or to close out any related open borrowings of Class A common stock, and may
use securities received from us or the Selling Stockholders in settlement of those derivatives to close out any related open borrowings
of our Shares. In addition, we or the Selling Stockholders may loan or pledge securities to a financial institution or other third party
that in turn may sell the securities using this prospectus and an applicable prospectus supplement. Such financial institution or other
third party may transfer its economic short position to investors in our securities or in connection with a concurrent offering of other
securities.
The
Selling Stockholders will act independently of us in making decisions with respect to the timing, manner, and size of each resale or
other transfer. There can be no assurance that the Selling Stockholders will sell any or all of the securities under this prospectus.
Further, we cannot assure you that the Selling Stockholders will not transfer, distribute, devise or gift the securities by other means
not described in this prospectus. In addition, any securities covered by this prospectus that qualify for sale under Rule 144 of the
Securities Act may be sold under Rule 144 rather than under this prospectus. A
Selling Stockholder that is an entity may elect to make
an in-kind distribution of the securities to its members, partners or shareholders pursuant to this prospectus by delivering a
prospectus. To the extent that such members, partners or shareholders are not affiliates
of ours, such members, partners or stockholders would thereby receive freely tradable shares of the securities pursuant to the distribution
through this prospectus.
All
securities we may offer, other than Class A common stock and the Lender Warrants, will be new issues of securities with no established
trading market. Any underwriters may make a market in these securities, but will not be obligated to do so and may discontinue any market
making at any time without notice. We cannot guarantee the liquidity of the trading markets for any securities.
Any
underwriter may be granted an option to purchase additional shares, and engage in stabilizing transactions, short-covering transactions
and penalty bids in accordance with Regulation M under the Exchange Act. An underwriters option to purchase additional shares
involves sales in excess of the offering size, which create a short position. Stabilizing transactions permit bids to purchase the underlying
security so long as the stabilizing bids do not exceed a specified maximum price. Syndicate-covering or other short-covering transactions
involve purchases of the securities, either through exercise of the option to purchase additional shares or in the open market after
the distribution is completed, to cover short positions. Penalty bids permit the underwriters to reclaim a selling concession from a
dealer when the securities originally sold by the dealer are purchased in a stabilizing or covering transaction to cover short positions.
Those activities may cause the price of the securities to be higher than it would otherwise be. If commenced, the underwriters may discontinue
any of the activities at any time.
Any
underwriters, dealers or agents that are qualified market makers on the Nasdaq may engage in passive market making transactions in our
Class A common stock on the Nasdaq in accordance with Regulation M under the Exchange Act, during the business day prior to the pricing
of the offering, before the commencement of offers or sales of the Class A common stock. Passive market makers must comply with applicable
volume and price limitations and must be identified as passive market makers. In general, a passive market maker must display its bid
at a price not in excess of the highest independent bid for such security; if all independent bids are lowered below the passive market
makers bid, however, the passive market makers bid must then be lowered when certain purchase limits are exceeded. Passive
market making may stabilize the market price of the securities at a level above that which might otherwise prevail in the open market
and, if commenced, may be discontinued at any time.
LEGAL
MATTERS
Unless
otherwise indicated in the applicable prospectus supplement, the validity of the securities offered hereby will be passed upon for us
by Sherman & Howard L.L.C. If the validity of the securities offered hereby in connection with offerings made pursuant to this prospectus
are passed upon by counsel for the underwriters, dealers or agents, if any, such counsel will be named in the prospectus supplement relating
to such offering.
EXPERTS
The
balance sheets of BioVie Inc. as of June 30, 2023 and 2022, and the related statements of operations and comprehensive loss, changes
in stockholders equity, and cash flows for each of the years then ended, have been audited by EisnerAmper LLP, independent
registered public accounting firm, as stated in their report which is incorporated by reference, which report includes an explanatory
paragraph about the existence of substantial doubt concerning the Companys ability to continue as a going concern. Such financial
statements have been incorporated by reference in reliance on the report of such firm given upon their authority as experts in accounting
and auditing.
LIMITATION
ON LIABILITY AND DISCLOSURE OF COMMISSION POSITION ON
INDEMNIFICATION FOR SECURITIES ACT LIABILITIES
Insofar
as indemnification for liabilities arising under the Securities Act may be permitted to our directors, officers and controlling persons
pursuant to the foregoing provisions, or otherwise, we have been advised that in the opinion of the SEC such indemnification is against
public policy as expressed in the Securities Act and is, therefore, unenforceable. In the event that a claim for indemnification against
such liabilities (other than the payment by the registrant of expenses incurred or paid by a director, officer or controlling person
of the registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person
in connection with the securities being registered, we will, unless in the opinion of our counsel the matter has been settled by controlling
precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by us is against public policy as
expressed in the Securities Act and will be governed by the final adjudication of such issue.
WHERE
YOU CAN FIND MORE INFORMATION
This
prospectus is part of the registration statement on Form S-3 we filed with the SEC under the Securities Act and does not contain all
the information set forth in the registration statement. Whenever a reference is made in this prospectus to any of our contracts, agreements
or other documents, the reference may not be complete and you should refer to the exhibits that are a part of the registration statement
or the exhibits to the reports or other documents incorporated by reference into this prospectus for a copy of such contract, agreement
or other document. Because we are subject to the information and reporting requirements of the Securities Exchange Act of 1934, as amended
(the Exchange Act), we file annual, quarterly and current reports, proxy statements and other information with the SEC.
Our SEC filings are available to the public over the Internet at the SECs website at http://www.sec.gov.
You
may also access our SEC filings at our website https://bioviepharma.com/. Our website and the information contained on, or that
can be accessed through, our website will not be deemed to be incorporated by reference in, and are not considered part of, this prospectus.
You should not rely on our website or any such information in making your decision whether to purchase our securities.
INFORMATION
INCORPORATED BY REFERENCE
We
have elected to incorporate certain information by reference into this prospectus. By incorporating by reference, we can disclose important
information to you by referring you to other documents we have filed or will file with the SEC. The information incorporated by reference
is deemed to be part of this prospectus, except for information incorporated by reference that is superseded by information contained
in this prospectus. This means that you must look at all of the SEC filings that we incorporate by reference to determine if any statements
in the prospectus or any document previously incorporated by reference have been modified or superseded. This prospectus incorporates
by reference the documents set forth below that we have previously filed with the SEC under the Exchange Act:
| ● | Our
Annual Report on Form 10-K for the year ended June 30, 2023, filed with the SEC on August
16, 2023, including any amendments or supplements thereto; |
| ● | Our
Current Reports on Form 8-K, filed with the SEC on October 5, 2022, November 10, 2022, December
6, 2022 (both filed on such date), December 7, 2022 December 15, 2022, December 23, 2022,
March 6, 2023, March 13, 2023, March 23, 2023 and April 7, 2023; and |
| ● | The
description of our Class A common stock contained in our registration on Form 8-A (File No.
001-39015) filed with the SEC on August 25, 2020, including any amendment or report filed
for the purpose of updating such description. |
All
documents subsequently filed by the Registrant with the SEC pursuant to Sections 13(a), 13(c), 14 and 15(d) of the Exchange Act after
the date of the initial filing of the registration statement and prior to effectiveness of the registration statement that contains this
prospectus and prior to the termination of the offering (except in each case the information contained in such document to the extent
furnish and not filed), shall be deemed to be incorporated by reference herein and to be a part hereof from
the date of filing of such documents.
Any
statement contained in a document incorporated or deemed to be incorporated by reference herein shall be deemed to be modified or superseded
for purposes of this Registration Statement to the extent that a statement contained herein, or in any other subsequently filed document
which also is incorporated or deemed to be incorporated by reference herein, modifies or supersedes such statement. Any such statement
so modified or superseded shall not be deemed, except as so modified or superseded, to constitute a part of this Registration Statement.
15,000,000 Shares of Class A Common Stock
Pre-funded Warrants to Purchase up to 6,000,000
Shares of Class A Common Stock
Warrants to Purchase up to 10,500,000 Shares of
Class A Common Stock
ThinkEquity
March 4, 2024
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