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UNITED STATES
SECURITIES AND EXCHANGE
COMMISSION
Washington, DC 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): December 4, 2023
Hepion
Pharmaceuticals, Inc.
(Exact name of registrant as specified in its
charter)
Delaware | |
001-36856 | |
46-2783806 |
(State or other jurisdiction
of incorporation or organization) |
|
(Commission
File Number) |
|
IRS Employer
Identification No.) |
399
Thornall Street, First Floor
Edison, NJ 08837
(Address of principal executive
offices)
Registrant’s telephone
number, including area code: (732) 902-4000
(Former name or former address, if changed since
last report)
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 |
|
HEPA |
|
Nasdaq
Capital 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
communication 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 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 x
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 5.02 | Departure of Directors or Principal Officers; Election of Directors;
Appointment of Principal Officers. |
On December 4,
2023, Dr. Robert Foster, the Company's CEO, resigned from the Company as CEO for personal reasons, effective immediately. In connection therewith, on December 4, 2023, Dr. Foster resigned from the Board
of Directors of the Company.
On December 4,
2023, the Board of Directors appointed John Cavan, the Company’s Chief Financial Officer, as interim Chief Executive Officer.
On December 4,
2023, Dr. Peter Wijngaard resigned from the Board of Directors of the Company. Dr. Wijngaard was a member of the Company’s
Audit Committee.
On December 6,
2023, the Company issued a press release announcing (i) that its Board of Directors has approved a strategic restructuring
plan, (ii) the resignation of Dr. Foster as the Company's CEO for personal reasons and (iii) the appointment of John Cavan as
interim Chief Executive Officer. A copy of the press release is furnished as Exhibit 99.1 to
this Form 8-K.
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.
Dated: December 7, 2023
|
HEPION PHARMACEUTICALS, INC. |
|
|
|
By: |
/s/
John Cavan |
|
|
John Cavan |
|
|
Interim Chief Executive Officer and Chief Financial Officer |
Exhibit 99.1
Hepion Pharmaceuticals
Announces Restructuring Plan to Enhance Shareholder Value and Management Changes
Restructuring
program purpose is to preserve capital and optimize clinical development program
Management
plans to continue to evaluate its Phase 2b ASCEND-NASH clinical trial taking in account current market environment
Cash
runway extended into Q2 2025
EDISON,
N.J., December 7, 2023 - Hepion Pharmaceuticals, Inc. (NASDAQ:HEPA),
a clinical stage biopharmaceutical company focused on Artificial Intelligence (“AI”)-driven therapeutic drug development
for the treatment of non-alcoholic steatohepatitis (“NASH”), fibrotic diseases, hepatocellular carcinoma (“HCC”),
and other chronic diseases, today announced that its Board of Directors has approved a strategic restructuring plan with the objective
of preserving capital by initially reducing operating costs by approximately 60% going forward. As a result, Hepion will incur a one-time
restructuring charge of approximately $400 – $800 thousand that will be recorded in the fourth quarter of 2023.
Additionally,
the Company has initiated a process to explore a range of strategic and financing alternatives focused on maximizing stockholder value
within the current financial environment and NASH drug development landscape. Currently 131 patients are being treated in our Phase 2b
(“ASCEND-NASH”) clinical trial. We intend on completing the treatment of such patients and will add additional patients once
the clinical trial is fully funded or a strategic transaction has been entered into.
Potential strategic
alternatives that may be considered by the Company as part of this process include an acquisition, merger, reverse merger, other business
combination, sale of assets, licensing, and other strategic transactions. The Company intends to pursue this process, however, there
can be no assurance that it will result in any agreements or transactions, or that, if completed, any agreements or transactions will
be successful. The Company does not expect to provide incremental updates during the evaluation process unless and until the Board of
Directors has concluded that disclosure is appropriate or required.
In addition, the Company
announced that Dr. Robert Foster, the Company’s CEO, resigned from the Company as CEO and director for personal reasons, effective
immediately. John Cavan, the Company’s CFO has been appointed as interim CEO.
“On
behalf of the Board, I would like to thank Robert for his many contributions to the Company in working to advance the development of
rencofilstat. Robert is leaving for personal reasons, and we wish him all the best,”
commented Gary S. Jacob, Ph.D., Chairman of the Hepion Board.
Dr.
Foster said “I sincerely enjoyed my tenure with the company over the past years. We put our hearts and souls into
bringing rencofilstat into the ongoing Phase 2b clinical trials in NASH, and I wish the very best for the continued successes of the
Company’s development program.”
With the organizational changes
announced today and its ongoing cost management efforts, the Company now expects its current cash, cash equivalents and investments will
be sufficient to fund its operations into Q2 2025.
About Hepion Pharmaceuticals
The Company's lead
drug candidate, rencofilstat, is a potent inhibitor of cyclophilins, which are involved in many disease processes. Rencofilstat has been
shown to reduce liver fibrosis and hepatocellular carcinoma tumor burden in experimental disease models and is currently in Phase 2 clinical
development for the treatment of NASH. In November 2021, the U.S. Food and Drug Administration (“FDA”) granted Fast
Track designation for rencofilstat for the treatment of NASH. That was followed in June 2022 by the FDA’s granting of Orphan
Drug designation to rencofilstat for the treatment of HCC.
Hepion has created
a proprietary Artificial Intelligence deep machine learning (“AI/ML”) platform designed to better understand disease processes
and identify patients that are rencofilstat responders. This AI/ML has the potential to shorten development timelines and increase the
observable differences between placebo and treatment groups. In addition, Hepion’s AI/ML can be used to drive its ongoing NASH
and HCC clinical development programs and identify other potential therapeutic indications for cyclophilin inhibition with rencofilstat.
Forward-Looking
Statements
Certain statements
in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements
may be identified by the use of forward-looking words such as “anticipate,” “believe,” “forecast,”
“estimated,” and “intend,” among others. These forward-looking statements are based on Hepion Pharmaceuticals’
current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ
materially from those indicated by such forward-looking statements. These factors include, but are not limited to, substantial competition;
our ability to continue as a going concern; our need for additional financing; uncertainties of patent protection and litigation; risks
associated with delays, increased costs and funding shortages caused by the COVID-19 pandemic; uncertainties with respect to lengthy
and expensive clinical trials, that results of earlier studies and trials may not be predictive of future trial results; uncertainties
of government or third party payer reimbursement; limited sales and marketing efforts and dependence upon third parties; and risks related
to failure to obtain FDA clearances or approvals and noncompliance with FDA regulations. As with any drug candidates under development,
there are significant risks in the development, regulatory approval, and commercialization of new products. There are no guarantees that
future clinical trials discussed in this press release will be completed or successful, or that any product will receive regulatory approval
for any indication or prove to be commercially successful. Hepion Pharmaceuticals does not undertake an obligation to update or revise
any forward-looking statement. Investors should read the risk factors set forth in Hepion Pharmaceuticals’ Form 10-K for the
year ended December 31, 2022, and other periodic reports filed with the Securities and Exchange Commission.
For further information,
please contact:
Veronica Della
Franco
Hepion Pharmaceuticals Investor Relations
732-902-4020
vdellafranco@hepionpharma.com
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