Item 8.01 Other
Events.
On March 4,
2020, the U.S. Securities and Exchange Commission (the “SEC”) issued an order under Section 36 (Release No. 34-88318)
of the Securities Exchange Act of 1934, as amended (“Exchange Act”), granting exemptions from specified provisions
of the Exchange Act and certain rules thereunder. On March 25, 2020, the order was modified and superseded by a new SEC order (Release
No. 34-88465), which provides conditional relief to public companies that are unable to timely comply with their filing obligations
as a result of the novel coronavirus (“COVID-19”) outbreak (the “SEC Order”). The SEC Order provides that
a registrant subject to the reporting requirements of Exchange Act Section 13(a) or 15(d), and any person required to make any
filings with respect to such registrant, is exempt from any requirement to file or furnish materials with the Commission under
Exchange Act Sections 13(a), 13(f), 13(g), 14(a), 14(c), 14(f), 15(d) and Regulations 13A, Regulation 13D-G (except for those provisions
mandating the filing of Schedule 13D or amendments to Schedule 13D), 14A, 14C and 15D, and Exchange Act Rules 13f-1, and 14f-1,
as applicable, if certain conditions are satisfied.
Hepion Pharmaceuticals,
Inc. (the “Company”) will be relying on the SEC Order to delay the filing of its Annual Report on Form 10-K for the
year ended December 31, 2019 (the “Report”) due to the circumstances related to COVID-19. In particular, COVID-19 has
caused severe disruptions in travel and transportation and limited access to the Company’s facilities resulting in limited
support from its staff. This has, in turn, delayed the Company’s ability to complete its annual review and prepare the Report.
Notwithstanding the foregoing, the Company expects to file the Report no later than May 14, 2020 (which is 45 days from the Report’s
original filing deadline of March 30, 2020).
In light of
the current COVID-19 pandemic, the Company will be including the following Risk Factor in its Report:
A pandemic, epidemic or
outbreak of an infectious disease, such as COVID-19, may materially and adversely affect our business and operations.
The
recent outbreak of COVID-19 originated in Wuhan, China, in December 2019 and has since spread to multiple countries, including
the United States and several European countries. On March 11, 2020, the World Health Organization declared the outbreak a pandemic.
The COVID-19 pandemic is affecting the United States and global economies and may affect our operations and those of third parties
on which we rely, including by causing disruptions in the supply of our product candidate and the conduct of current and future
clinical trials. In addition, the COVID-19 pandemic may affect the operations of the FDA and other health authorities, which could
result in delays of reviews and approvals, including with respect to our product candidates. The evolving COVID-19 pandemic is
also likely to directly or indirectly impact the pace of enrollment in our CRV431 clinical trials for at least the next several
months and possibly longer as patients may avoid or may not be able to travel to healthcare facilities and physicians' offices
unless due to a health emergency and clinical trial staff can no longer get to the clinic. Such facilities and offices may also
be required to focus limited resources on non-clinical trial matters, including treatment of COVID-19 patients, and may not be
available, in whole or in part, for clinical trial services related to CRV431. Additionally, while the potential economic impact
brought by, and the duration of the COVID-19 pandemic is difficult to assess or predict, the impact of the COVID-19 pandemic on
the global financial markets may reduce our ability to access capital, which could negatively impact our short-term and long-term
liquidity. The ultimate impact of the COVID-19 pandemic is highly uncertain and subject to change. We do not yet know the full
extent of potential delays or impacts on our business, financing or clinical trial activities or on healthcare systems or the global
economy as a whole. However, these effects could have a material impact on our liquidity, capital resources, operations and business
and those of the third parties on which we rely.
Cautionary Note Regarding Forward-Looking
Statements
This Current Report on Form 8-K
contains statements that are forward-looking statements within the meaning of the Private Securities Litigation Reform Act of
1995. These forward-looking statements relate to expectations or forecasts for future events, including, without limitation,
our future financial or business performance or strategies, results of operations or financial condition. These statements
may be preceded by, followed by or include the words “may,” “might,” “should,”
“estimate,” “plan,” “project,” “forecast,” “intend,”
“expect,” “anticipate,” “believe,” “seek,” “continue,”
“target” or similar expressions. These forward-looking statements are based on information available to us as of
the date they were made and involve a number of risks and uncertainties which may cause them to turn out to be wrong.
Accordingly, forward-looking statements should not be relied upon as representing our views as of any subsequent date, and we
do not undertake any obligation to update forward-looking statements to reflect events or circumstances after the date they
were made, whether as a result of new information, future events or otherwise, except as may be required under applicable
securities laws. As a result of a number of known and unknown risks and uncertainties, including the unprecedented impact of
COVID-19 pandemic on our business, employees, consultants, service providers, subcontractors and supply chain, stockholders,
investors and other stakeholders, our actual results or performance may be materially different from those expressed or
implied by these forward-looking statements. Please refer to our Form 10-K to be filed with the SEC as well as any subsequent
filings made by us pursuant to the Exchange Act, each of which is available on the SEC’s website (www.sec.gov), for a
full discussion of the risks and other factors that may impact any forward-looking statements in this presentation.