Current Report Filing (8-k)
19 Juillet 2022 - 10:07PM
Edgar (US Regulatory)
0000786947
false
0000786947
2022-07-18
2022-07-18
iso4217:USD
xbrli:shares
iso4217:USD
xbrli:shares
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 18, 2022
___________________________________________________________
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 Pink |
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 (17CFR 240.14d-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 18, 2022, Acura Pharmaceuticals, Inc.
(“we” “Acura” or the “Company”), received a $150,000 loan from John Schutte and to date, we have received
a total of $1,275,000. In connection with the $150,000 loan, we issued an unsecured promissory note, or the Schutte Note, in that principal
amount to him. The Schutte Note 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 Schutte 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 Mr. Schutte will be used
for operations over the course of the next several weeks. There can be no assurance we will be successful in receiving additional financing.
In the absence of the receipt of additional financing by mid-August 2022, 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 Schutte
Note under Item 1.01 of this Current Report on Form 8-K shall not be deemed an acknowledgement that the Schutte Note is a material agreement
not made, or deemed not to be made, in the ordinary course of our business.
Mr. Schutte directly owns approximately 14% of
our common stock as of January 30, 2022. Mr. Schutte also controls MainPointe Pharmaceuticals, LLC and is an investor in Abuse Deterrent
Pharma, LLC (“AD Pharma”). AD Pharma directly owns approximately 66% of our common stock as of January 30, 2022, which does
not include their warrant to purchase 10.0 million shares of the Company’s common stock.
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; |
| · | 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
Pursuant to the requirements of the Securities
Exchange Act of 1934, the Registrant has duly caused this Current Report to be signed on its behalf by the undersigned thereunto duly
authorized.
Date: July 19, 2022 |
ACURA PHARMACEUTICALS, INC. |
|
|
|
By: |
/s/ Peter A. Clemens |
|
|
Peter A. Clemens |
|
|
Senior Vice President & Chief Financial Officer |
Acura Pharmaceuticals (CE) (USOTC:ACUR)
Graphique Historique de l'Action
De Déc 2024 à Jan 2025
Acura Pharmaceuticals (CE) (USOTC:ACUR)
Graphique Historique de l'Action
De Jan 2024 à Jan 2025