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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):
July 10, 2023
___________________________________________________________
ACURA PHARMACEUTICALS, INC.
(Exact Name of Registrant as specified in its Charter)
___________________________________________________________
New York | 1-10113 | 11-0853640 |
(State or other jurisdiction of | (Commission File Number) | (I.R.S.
Employer |
incorporation or organization) | | Identification Number) |
616 N. North Court, Suite 120
Palatine, Illinois 60067
(Address of principal executive offices) (Zip code)
(847) 705-7709
(Registrant’s telephone number, including
area code)
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, $0.01 par value per share |
ACUR |
OTC Market – OTC Expert Market
|
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 (17CFR240.14d-2(b)) |
| ¨ | Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17CFR 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. ¨
Item 1.01 - Entry into a Material Definitive Agreement.
On July 10, 2023 we received a $200,000 loan from
Abuse Deterrent Pharma, LLC (“AD Pharma”). This loan combined with previous loans made to the Company and with the $2,319,279
under the November 10, 2022 Amended Consolidated and Restated Secured Promissory Note, now totals $3,669,279, bears interest at 5.25%
and matures on December 31, 2023, at which time all principal and interest is due. Events of default under the Note include, among other
items, bankruptcy events, failure to pay interest and principal when due and such failure continues for 5 days, and if Acura is generally
not, or is unable to, or admits in writing its inability to, pay its debts as they become due. If any amount payable hereunder is not
paid when due (without regard to any applicable grace periods), whether at stated maturity, by acceleration, or otherwise, including upon
an event of default, such overdue amount shall bear interest at the rate per annum of 7.5% from the date of such non-payment until such
amount is paid in full.
The funding provided by AD Pharma will be used
for operations through mid-August 2023. There can be no assurance we will be successful in receiving additional financing. In the absence
of the receipt of additional financing by the mid-August 2023, we will be required to scale back or terminate operations and/or seek protection
under applicable bankruptcy laws. This could result in a complete loss of shareholder value in the Company. Even assuming we are successful
in securing additional sources of financing to fund continued operations, there can be no assurance that the proceeds of such financing
will be sufficient to fund operations until such time, if at all, that we generate sufficient revenue from our products and product candidates
to sustain and grow our operation.
The inclusion of a description of the Note under
Item 1.01 of this Current Report on Form 8-K shall not be deemed an acknowledgement that the Note is a material agreement not made, or
deemed not to be made, in the ordinary course of our business.
At July 1, 2023, AD Pharma directly owns approximately
66% of the outstanding common stock of the Company. The ownership percentage of the Company held by AD Pharma does not include their warrant
to purchase 10.0 million shares of common stock of the Company. AD Pharma is an entity controlled by Mr. Schutte, of which Mr. Schutte
is the managing partner and investor. At July 1, 2023, Mr. Schutte directly owns approximately 14% of the outstanding common stock of
the Company.
Item 2.01 – Completion of Acquisition
or Disposition of Assets
The contents of Item 1.01 are incorporated herein by reference.
Item 2.03 - Creation of a Direct Financial
Obligation or an Obligation under an Off-Balance Sheet Arrangement of a Registrant
The contents of Item 1.01 are incorporated herein by reference.
Forward-Looking Statements
Statements in this Current
Report constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking
statements involve known and unknown risks, uncertainties and other factors which may cause our actual results, performance or achievements
to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements.
Forward-looking statements
may include, but are not limited to:
| · | our
ability to fund or obtain funding for our continuing operations, including the development of our products utilizing our LIMITx and IMPEDE
technologies; |
| · | whether
we will receive FDA acceptance for an NDA for LTX-03 by the target date, currently November 30, 2023; |
| · | whether
our licensees will terminate the license prior to commercialization; |
| · | the
expected results of clinical studies relating to LTX-03 or any successor product candidate, the date by which such studies will complete
and the results will be available and whether any product candidate will ultimately receive FDA approval; |
| · | the
ability of LTX-03 single tablets to achieve bioequivalence or to demonstrate efficacy in a clinical study; |
| · | whether
our licensing partners will develop any additional products and utilize Acura for such development; |
| · | whether
LIMITx will retard the release of opioid active ingredients as dose levels increase; |
| · | whether
the extent to which products formulated with the LIMITx technology mitigate respiratory depression risk will be determined sufficient
by the FDA; |
| · | our
and our licensee’s ability to successfully launch and commercialize our products and technologies; |
| · | our
and our licensee’s ability to obtain necessary regulatory approvals and commercialize products utilizing our technologies; |
| · | the
market acceptance of, timing of commercial launch and competitive environment for any of our products; |
| · | our
ability to develop and enter into additional license agreements for our product candidates using our technologies; |
| · | the
ability to avoid infringement of patents, trademarks and other proprietary rights of third parties; |
| · | the
ability of our patents to protect our products from generic competition and our ability to protect and enforce our patent rights in any
paragraph IV patent infringement litigation; |
| · | the
adequacy of the development program for our product candidates, including whether additional clinical studies will be required to support
an NDA and FDA approval of our product candidates; |
| · | changes
in regulatory requirements; |
| · | adverse
safety findings relating to our commercialized products or product candidates in development; |
| · | whether
or when we are able to obtain FDA approval of labeling for our product candidates for the proposed indications and whether we will be
able to promote the features of our technologies; and |
| · | whether
our product candidates will ultimately perform as intended in commercial settings. |
In
some cases, you can identify forward- looking statements by terms such as "may," “will”, "should," "could,"
"would," "expects," "plans," "anticipates," "believes," "estimates," “indicates”,
"projects," “predicts," "potential" and similar expressions intended to identify forward-looking statements.
These statements reflect our current views with respect to future events and are based on assumptions and subject to risks and uncertainties.
Given these uncertainties, you should not place undue reliance on these forward-looking statements. We discuss many of these risks in
greater detail in our filings with the Securities and Exchange Commission.
Item 9.01 - Financial Statements and Exhibits
SIGNATURES
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 thereunto duly authorized.
|
ACURA PHARMACEUTICALS, INC. |
|
|
|
By: |
/s/
Peter A. Clemens |
|
|
Peter A. Clemens |
|
|
Senior Vice President & Chief Financial Officer |
Date: July 13, 2023
Exhibit 99.1
Amended
Loan Schedule to Secured Promissory Note dated November 10, 2022
between Acura Pharmaceuticals, Inc and Abuse Deterrent Pharma,
LLC
| |
Date | |
Principal | | |
Aggregated
Principal | |
Original Secured Promissory Note | |
11/10/2022 | |
$ | 2,319,279 | | |
$ | 2,319,279 | |
Additional loans to be included: | |
| |
| | | |
| | |
Loan #1 | |
12/22/2022 | |
$ | 250,000 | | |
$ | 2,569,279 | |
Loan #2 | |
1/19/2023 | |
$ | 250,000 | | |
$ | 2,819,279 | |
Loan #3 | |
2/22/2023 | |
$ | 250,000 | | |
$ | 3,069,279 | |
Loan #4 | |
3/20/2023 | |
$ | 250,000 | | |
$ | 3,319,279 | |
Loan #5 | |
5/19/2023 | |
$ | 150,000 | | |
$ | 3,469,279 | |
Loan #6 | |
7/10/2023 | |
$ | 200,000 | | |
$ | 3,669,279 | |
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Acura Pharmaceuticals (CE) (USOTC:ACUR)
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