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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported):
February 8, 2024
Applied DNA Sciences, Inc.
(Exact name of registrant as specified in its charter)
Delaware |
001-36745 |
59-2262718 |
(State or other jurisdiction
of incorporation) |
(Commission File Number) |
(IRS Employer
Identification No.) |
50 Health Sciences Drive
Stony Brook, New York 11790
(Address of principal executive offices; zip code)
Registrant’s telephone number, including
area code:
631-240-8800
N/A
(Former name or former address, if changed since
last report)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Indicate by check mark whether the registrant
is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the
Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company ¨
If an emerging growth company, indicate by check
mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting
standards provided pursuant to Section 13(a) of the Exchange Act. ¨
Securities registered pursuant to Section 12(b)
of the Act:
Title of each class |
|
Trading Symbol(s) |
|
Name of each exchange on which registered |
Common Stock, $0.001 par value |
|
APDN |
|
The Nasdaq Stock Market |
Item 2.02 Results of Operations and Financial Condition.
On February 8, 2024, Applied DNA Sciences, Inc. (“Applied DNA
Sciences” or the “Company”) issued a press release announcing its results of operations for the three-month period ended
December 31, 2023. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
The information furnished pursuant to this Item 2.02, including Exhibit
99.1, shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange
Act”), or otherwise subject to the liabilities under that Section and shall not be deemed to be incorporated by reference into any
filing of the Company under the Securities Act of 1933 or the Exchange Act, except as shall be expressly set forth by specific reference
in such filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits
SIGNATURE
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned hereunto duly authorized.
Date: February 8, 2024 |
APPLIED DNA SCIENCES, INC. |
|
|
|
By: |
/s/ James A. Hayward |
|
Name: |
James A. Hayward |
|
Title: |
Chief Executive Officer |
EXHIBIT INDEX
Exhibit 99.1
Applied DNA Announces First Quarter Fiscal Year
2024
Financial Results
- Company On Track to
Initiate First-Phase GMP Production Capacity for mRNA Critical Starting Materials During First Half of Calendar 2024, Projects Initial
Facility Capacity to Enable up to $15 Million1 of Linea IVT Revenue2 Annually -
- Conference Call/Webcast
Scheduled for Today at 4:30 PM ET -
STONY BROOK, N.Y. – February
8, 2024 - Applied DNA Sciences, Inc. (NASDAQ: APDN) (“Applied DNA” or the “Company”), a leader in
PCR-based DNA technologies, today announced consolidated financial results for its first fiscal quarter ended December 31, 2023. The
Company’s Form 10-Q can be viewed at https://investors.adnas.com/sec-filings/.
“We made substantial progress
in advancing the commercialization of our Linea™ IVT platform and the availability of GMP capacity for the manufacture of critical
starting material for mRNA therapeutics during the past quarter,” stated Dr. James A. Hayward, president and CEO of Applied DNA.
“Our efforts centered on establishing and implementing new quality systems for GMP manufacturing to meet our customer requirements
at a scale sufficient for use through clinical-stage mRNA therapy development. In addition, we initiated a scale-up manufacturing project
for our Linea™ RNA polymerase (RNAP) with an enzyme manufacturer to optimize the enzyme’s production for commercial-scale
use. We also secured our first CDMO partner to validate the commercial scale-up of Linea IVT within a cGMP workflow setting.
“In parallel, we expanded our sales pipeline
and active projects with the addition of new research and development-stage customers for Linea IVT that can serve as the basis for potential
long-term supply agreements as customers’ therapies enter toxicology, pharmacokinetics, and early-stage clinical development,”
continued Dr. Hayward. “We generated data readouts that further substantiate the capacity of Linea IVT to create equal or
greater RNA yields with double-stranded RNA contamination at levels 10x-50x lower than those found using conventional mRNA production
methods. Feedback to-date on our Linea IVT and Linea DNA platforms has been positive, having completed multiple successful customer evaluations
within the quarter. Particularly noteworthy, we completed an evaluation with a clinical stage mRNA customer in which our IVT templates
meet or exceeded all customer quality metrics with manufacturing speed that exceeded all other IVT template sources being evaluated by
the customer.
1Based
on company internal modeling utilizing current pricing projections and industry figures
2 Linea IVT revenue
is comprised of Linea DNA IVT templates, Linea RNAP and technology license royalty
Concluded Dr. Hayward, “Supplying
both DNA template and RNA polymerase positions us to capture a greater percentage of the economics of mRNA therapy production that we
believe establishing our GMP production capacity will unlock. After the close of the quarter, we completed an equity offering that supports
the initial phase of our GMP plan and timeline for critical starting materials in the production of mRNA. Slated to come online during
first half of calendar 2024 and based on internal modeling, current pricing projections, and industry figures, we project our GMP facility,
with an initial footprint of less than 1,000 square feet, to enable annual total Linea IVT revenues of up to $15 million. We believe
our manufacturing workflow is highly reproducible, allowing us to scale our production facilities to meet incremental customer demand
quickly. Looking ahead, we will continue to prioritize the commercialization of our Linea IVT and Linea DNA platforms and rationalize
our cost structure in support of our biotherapeutic goals.”
Summary First Quarter Fiscal 2024 Financial Results:
| · | Total revenues were approximately $891 thousand for the three-month period December 31, 2023,
compared to $5.3 million for the same period in the prior fiscal year. The decrease in revenue of approximately $4.4 million was due
to an expected decline in COVID-19 testing services revenue of $4.2 million driven primarily by cancelation of the testing contract
with City University of New York (CUNY) in June 2023. The decrease was also due to a reduction in product revenue of $209 thousand
primarily related to a decline year-over-year in cotton DNA tagging revenue in our DNA Tagging and Security Products and Services
segment. |
| · | Gross profit for the
three-month period ended December 31, 2023, was $231 thousand, compared to $2.4 million for
the three-month period ended December 31, 2022. The gross profit percentage was 26% and 45%
for the three-month periods ended December 31, 2023, and 2022, respectively. The decline
in gross profit percentage was primarily the result of a decline in gross profit percentage
for our MDx (Molecular Diagnostics) testing services segment specifically related to decreased
COVID-19 testing volumes year over year. To a lesser extent, the decline in gross profit
percentage was due to lower product revenues during the three-month period ended December
31, 2023, as compared to the same period in the prior fiscal year. The lower volume of product
revenues in the current period were not able to fully absorb the fixed costs that are included
in cost of product revenues. |
| · | Operating expenses
increased to $4.0 million for the three-month period ended December 31, 2023, as compared
to $3.6 million for the first quarter of fiscal 2023. The increase in operating expenses
is the result of an increase in selling, general and administrative expenses of approximately
$459 thousand. The increase in SG&A expenses relates
to the prior three-month period having a credit in bad debt expense of approximately $290
thousand, from a customer balance that was fully reserved and was subsequently collected
during the three-month period ended December 31, 2023. The remainder of the increase
is attributable to an increase in stock-based compensation expense of $247 thousand. The
increase in stock-based compensation expense primarily relates to the timing of the annual
non-employee board of director grant that vests one-year from the date of grant during the
second quarter of fiscal 2023. These increases were
offset by a decrease in payroll of approximately $107 thousand. |
| · | Loss from operations was $3.8 million for the three-month period ended December 31, 2023, compared
to $1.2 million for the first quarter of 2023. |
| · | Excluding non-cash
expenses, Adjusted EBITDA was a negative $3.2 million for the three-month period ended December
31, 2023, compared to a negative $1.1 million for the same period in fiscal 2023. |
| · | Cash
and cash equivalents stood at $3.4 million on December 31, 2023, compared with $7.2 million
as of September 30, 2023. |
| | |
| | On February 2, 2024, the Company closed on a registered direct offering with institutional investors
for gross proceeds of $3.44 million. In a concurrent private placement, the Company issued 11,288,122 unregistered
warrants with an exercise price of $0.609 per warrant share. If these warrants were to be exercised assuming
stockholder approval is obtained, it would result in additional gross proceeds of $6.87 million. The Company
also agreed to reduce the exercise price of warrants previously issued to the investors as well as other
certain other prior investors with exercise prices ranging from $1.29 to $4.00 per warrant to $0.609 per
warrant. The Company further agreed to extend the expiration dates for such warrants to August 2028. The
foregoing reductions of the exercise price and extension of expiration dates of such warrants is subject
to stockholder approval and if such warrants were to be exercised, it would result in additional gross
proceeds of $1.86 million. |
First Quarter Fiscal 2024 Conference Call Information
The Company will hold a conference call and webcast to discuss its
first quarter of fiscal year 2024 financial results on Thursday, February 8, 2024, at 4:30 PM ET. To participate in the conference call,
please follow the instructions below. While every attempt will be made to answer investors’ questions on the Q&A portion of
the call, not all questions may be answered.
To Participate, please ask to be joined to the ‘Applied DNA
Sciences’ call:
| · | Domestic
callers (toll free): 844-887-9402 |
| | |
| · | International
callers: 412-317-6798 |
| | |
| · | Canadian
callers (toll free): 866-605-3852 |
Live and replay of webcast: https://event.choruscall.com/mediaframe/webcast.html?webcastid=UXIQvhHk
Telephonic replay (available 1 hour following the conclusion of
the live call through February 15, 2024):
| · | Domestic
callers (toll free): 1-877-344-7529 |
| | |
| · | Canadian
callers (toll free): 1-855-669-9658 |
| | |
| · | Participant
Passcode: 3086410 |
An accompanying slide presentation that will be embedded in the webcast
can be accessed under ‘News & Events’ tab and ‘Company Events’ section of the Applied DNA investor relations
website at https://investors.adnas.com/
About the Linea™ DNA and Linea™ IVT Platforms
The Linea DNA platform is a completely cell-free DNA production platform
founded on the Company’s long-standing expertise in the large-scale enzymatic production of DNA. Capable of producing DNA in quantities
ranging from milligrams to grams, the Linea DNA platform can produce high-fidelity DNA constructs ranging from 100bp to 20kb in size.
The DNA produced via the Linea DNA platform is free of the adventitious DNA sequences found in other sources of DNA, is rapidly scalable,
and provides for simple chemical modification of DNA constructs.
The Linea IVT platform combines DNA IVT templates manufacturing via
the Linea DNA platform with a proprietary Linea™ RNAP to enable mRNA and saRNA manufacturers to produce better mRNA faster, with
advantages over conventional mRNA production, including: 1) the elimination of plasmid DNA as a starting material; 2) the prevention
or reduction of dsRNA contamination; and 3) simplified mRNA production workflows.
Information about Non-GAAP Financial Measures
As used herein, “GAAP” refers to accounting principles
generally accepted in the United States of America. To supplement our condensed consolidated financial statements prepared and presented
in accordance with GAAP, this earnings release includes Adjusted EBITDA, which is a non-GAAP financial measure as defined in Rule 101
of Regulation G promulgated by the Securities and Exchange Commission. Generally, a non-GAAP financial measure is a numerical measure
of a company’s historical or future performance, financial position, or cash flows that either excludes or includes amounts that
are not normally excluded or included in the most directly comparable measure calculated and presented in accordance with GAAP. The presentation
of this non-GAAP financial information is not intended to be considered in isolation or as a substitute for, or superior to, the financial
information presented in accordance with GAAP. We use this non-GAAP financial measure for internal financial and operational decision-making
purposes and as a means to evaluate period-to-period comparisons of the performance and results of operations of our core businesses.
Our management believes that these non-GAAP financial measures provide meaningful supplemental information regarding the performance
of our businesses by excluding non-cash expenses that may not be indicative of our recurring operating results. We believe this non-GAAP
financial measure is useful to investors as they allow for greater transparency with respect to key metrics used by management in its
financial and operational decision making.
“EBITDA”- is defined as earnings (loss) before interest
expense, income tax expense and depreciation and amortization expense.
“Adjusted EBITDA”- is defined as EBITDA adjusted to exclude
(i) stock-based compensation and (ii) other non-cash expenses.
About Applied DNA Sciences
Applied DNA Sciences is a biotechnology company
developing technologies to produce and detect deoxyribonucleic acid (“DNA”). Using the polymerase chain reaction (“PCR”)
to enable both the production and detection of DNA, we operate in three primary business markets: (i) the enzymatic manufacture of synthetic
DNA for use in the production of nucleic acid-based therapeutics and, through our recent acquisition of Spindle Biotech, Inc. (“Spindle”),
the development and sale of a proprietary RNA polymerase (“RNAP”) for use in the production of mRNA therapeutics; (ii) the
detection of DNA and RNA in molecular diagnostics and genetic testing services; and (iii) the manufacture and detection of DNA for industrial
supply chain security services.
Visit adnas.com for more information. Follow us on Twitter
and LinkedIn. Join our mailing list.
The Company’s common stock is listed on NASDAQ under ticker
symbol ‘APDN,’ and its publicly traded warrants are listed on OTC under ticker symbol ‘APPDW.’
Forward-Looking Statements
The statements made by Applied
DNA in this press release may be “forward-looking” in nature within the meaning of Section 27A of the Securities Act of 1933,
Section 21E of the Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. Forward-looking statements
describe Applied DNA’s future plans, projections, strategies, and expectations, and are based on assumptions and involve a number
of risks and uncertainties, many of which are beyond the control of Applied DNA. Actual results could differ materially from those projected
due to its history of net losses, limited financial resources, unknown future demand for its biotherapeutics products
and services, our unknown ability to procure additional financing to build incremental GMP manufacturing facility, the unknown amount
of revenues and profits that will result from our Linea IVT and or Linea DNA platforms, limited market acceptance for its supply chain
security products and services, the declining demand for Applied DNA’s COVID-19 testing services, the fact that there has never
been a commercial drug product utilizing PCR-produced DNA technology and/or the Linea IVT platform approved for therapeutic use, and
various other factors detailed from time to time in Applied DNA’s SEC reports and filings, including its Annual Report on
Form 10-K, as amended, filed on December 7, 2023 and Quarterly Report on Form 10-Q filed on February 8, 2024 and other reports it
files with the SEC, which are available at www.sec.gov. Applied DNA undertakes no obligation to update publicly any forward-looking
statements to reflect new information, events, or circumstances after the date hereof or to reflect the occurrence of unanticipated events,
unless otherwise required by law.
Investor Relations contact: Sanjay M. Hurry, 917-733-5573,
sanjay.hurry@adnas.com
Web: www.adnas.com
Twitter: @APDN
- Financial Tables Follow -
APPLIED DNA SCIENCES,
INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
| |
December 31, | | |
September 30, | |
| |
2023 | | |
2023 | |
ASSETS | |
(unaudited) | | |
| |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 3,359,045 | | |
$ | 7,151,800 | |
Accounts receivable, net of allowance of $75,000 at December 31, 2023 and September 30, 2023, respectively | |
| 450,757 | | |
| 255,502 | |
Inventories | |
| 377,291 | | |
| 330,027 | |
Prepaid expenses and other current assets | |
| 402,953 | | |
| 389,241 | |
Total current assets | |
| 4,590,046 | | |
| 8,126,570 | |
| |
| | | |
| | |
Property and equipment, net | |
| 539,319 | | |
| 838,270 | |
Other assets: | |
| | | |
| | |
Restricted cash | |
| 750,000 | | |
| 750,000 | |
Intangible assets | |
| 2,698,975 | | |
| 2,698,975 | |
Operating right of use asset | |
| 1,117,317 | | |
| 1,237,762 | |
Capitalized transaction costs | |
| 217,553 | | |
| — | |
Total assets | |
$ | 9,913,210 | | |
$ | 13,651,577 | |
| |
| | | |
| | |
LIABILITIES AND EQUITY | |
| | | |
| | |
| |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable and accrued liabilities | |
$ | 2,023,876 | | |
$ | 2,270,388 | |
Operating lease liability, current | |
| 510,028 | | |
| 498,598 | |
Deferred revenue | |
| 54,035 | | |
| 76,435 | |
Total current liabilities | |
| 2,587,939 | | |
| 2,845,421 | |
| |
| | | |
| | |
Long term accrued liabilities | |
| 31,467 | | |
| 31,467 | |
Deferred revenue, long term | |
| 227,999 | | |
| 194,000 | |
Operating lease liability, long term | |
| 607,288 | | |
| 739,162 | |
Deferred tax liability, net | |
| 684,115 | | |
| 684,115 | |
Warrants classified as a liability | |
| 1,646,000 | | |
| 4,285,000 | |
Total liabilities | |
| 5,784,808 | | |
| 8,779,165 | |
| |
| | | |
| | |
Commitments and contingencies (Note G) | |
| | | |
| | |
| |
| | | |
| | |
Applied DNA Sciences, Inc. stockholders’ equity: | |
| | | |
| | |
Preferred stock, par value $0.001 per share; 10,000,000 shares authorized; -0-
shares issued and outstanding as of December 31, 2023 and September 30 2023, respectively | |
| — | | |
| — | |
Series A Preferred stock, par value $0.001 per share; 10,000,000 shares
authorized; -0- issued and outstanding as of December 31, 2023 and September 30, 2023, respectively | |
| — | | |
| — | |
Series B Preferred stock, par value $0.001 per share; 10,000,000 shares authorized; -0- issued and outstanding as of December 31, 2023 and September 30, 2023, respectively | |
| — | | |
| — | |
| |
| | | |
| | |
Common stock, par value $0.001 per share; 200,000,000 shares authorized as of
December 31, 2023 and September 30, 2023, 13,721,820 and 13,658,520 shares issued and outstanding as of December 31, 2023 and
September 30, 2023, respectively | |
| 13,722 | | |
| 13,659 | |
Additional paid in capital | |
| 307,848,612 | | |
| 307,384,647 | |
Accumulated deficit | |
| (303,630,004 | ) | |
| (302,447,147 | ) |
Applied DNA Sciences, Inc. stockholders’ equity | |
| 4,232,330 | | |
| 4,951,159 | |
Noncontrolling interest | |
| (103,928 | ) | |
| (78,747 | ) |
Total equity | |
| 4,128,402 | | |
| 4,872,412 | |
| |
| | | |
| | |
Total liabilities and equity | |
$ | 9,913,210 | | |
$ | 13,651,577 | |
APPLIED DNA SCIENCES, INC.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(unaudited)
| |
Three Months Ended December 31, | |
| |
2023 | | |
2022 | |
Revenues | |
| | | |
| | |
Product revenues | |
$ | 307,317 | | |
$ | 516,396 | |
Service revenues | |
| 247,147 | | |
| 232,061 | |
Clinical laboratory service revenues | |
| 336,700 | | |
| 4,514,295 | |
Total revenues | |
| 891,164 | | |
| 5,262,752 | |
| |
| | | |
| | |
Cost of product revenues | |
| 282,545 | | |
| 365,378 | |
Cost of clinical laboratory service revenues | |
| 377,522 | | |
| 2,519,691 | |
Total cost of revenues | |
| 660,067 | | |
| 2,885,069 | |
| |
| | | |
| | |
Gross profit | |
| 231,097 | | |
| 2,377,683 | |
| |
| | | |
| | |
Operating expenses: | |
| | | |
| | |
Selling, general and administrative | |
| 3,084,348 | | |
| 2,625,357 | |
Research and development | |
| 935,815 | | |
| 971,304 | |
Total operating expenses | |
| 4,020,163 | | |
| 3,596,661 | |
| |
| | | |
| | |
LOSS FROM OPERATIONS | |
| (3,789,066 | ) | |
| (1,218,978 | ) |
| |
| | | |
| | |
Interest income | |
| 33,323 | | |
| 3,686 | |
Unrealized gain (loss) on change in fair value of warrants classified as a liability | |
| 2,639,000 | | |
| (2,637,800 | ) |
Other (expense) income, net | |
| (13,538 | ) | |
| 8,846 | |
| |
| | | |
| | |
Loss before provision for income taxes | |
| (1,130,281 | ) | |
| (3,844,246 | ) |
| |
| | | |
| | |
Provision for income taxes | |
| — | | |
| — | |
| |
| | | |
| | |
NET LOSS | |
$ | (1,130,281 | ) | |
$ | (3,844,246 | ) |
| |
| | | |
| | |
Less: Net loss attributable to noncontrolling interest | |
| 25,181 | | |
| 874 | |
NET LOSS attributable to Applied DNA Sciences, Inc. | |
$ | (1,105,100 | ) | |
$ | (3,843,372 | ) |
Deemed dividend related to warrant modifications | |
| (77,757 | ) | |
| — | |
NET LOSS attributable to common stockholders | |
$ | (1,182,857 | ) | |
$ | (3,843,372 | ) |
Net loss per share attributable to common stockholders-basic and diluted | |
$ | (0.09 | ) | |
$ | (0.30 | ) |
| |
| | | |
| | |
Weighted average shares outstanding- basic and diluted | |
| 13,673,433 | | |
| 12,908,520 | |
APPLIED DNA SCIENCES, INC.
CALCULATION AND RECONCILIATION OF ADJUSTED
EBITDA
(unaudited)
| |
Three Month Period Ended
December 31, | |
| |
2023 | | |
2022 | |
Net Loss | |
$ | (1,130,281 | ) | |
$ | (3,844,246 | ) |
Interest expense (income), net | |
| (33,323 | ) | |
| (3,686 | ) |
Depreciation and amortization | |
| 298,951 | | |
| 338,918 | |
Provision for bad debt | |
| - | | |
| (290,022 | ) |
Unrealized gain on change in fair value of Common Warrants | |
| (2,639,000 | ) | |
| 2,637,800 | |
Stock based compensation expense | |
| 340,705 | | |
| 93,748 | |
Total non-cash items | |
| (2,032,667 | ) | |
| 2,776,758 | |
Consolidated Adjusted EBITDA (loss) | |
$ | (3,162,948 | ) | |
$ | (1,067,488 | ) |
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Applied DNA Sciences (NASDAQ:APDN)
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