OTC: HEPA

accounted for this transaction as an asset acquisition. The total consideration of $815,045, including the $19,146 of transaction fees,
was allocated between purchased in-process research and development and Intangibles for the assets with CE mark in the EU. The portion
allocated to in-process research and development was $412,299 and it was expensed upon the completion of the transaction, as research
and development cost. We did not recognize any contingent consideration (milestone payments) given the low probability of meeting those
targets. Royalties will be recognized when earned.

In
accordance with ASC 360-10-35-21, a long-lived asset (asset group) shall be tested for recoverability whenever events or changes in circumstances
indicate that its carrying amount may not be recoverable. We tested the asset for impairment during the reporting period, noting there
were triggering events related to delayed timing to market resulting in an adverse effect on estimated cashflow over the next two years.
Given that the license agreement requires both parties to agree to renewal after the initial two years, we projected the estimated cashflows
for the first two years for the assets available for sales in eligible markets, noting the projected cashflow will not be enough to recover
the allocated cost in the first two years of the license agreement. The total impairment loss recorded was $402,746. Therefore, the total
cost related to the New Day licensing agreement was expensed.

On
May 26, 2025, we entered into a patent and associated assets acquisition agreement (the “Agreement”) with Panetta Partners
Limited (“Panetta”) whereby Panetta purchased from us all patent assets, knowhow, clinical trial data and drug product relating
to Rencofilstat (formerly CRV431) for a nominal amount. There was no gain or loss resulting from this transaction. Panetta also assumed
all contingent consideration obligations to the predecessor company’s shareholders. Pursuant to the Agreement, Panetta agreed to
provide a contingent value right (“CVR”) to our stockholders to receive one or more contingent payments upon the achievement
of certain milestones as set forth below:

a)
a payment of US$500,000
on the regulatory approval by the US Food and Drug Administration of the first new drug application for Rencofilstat (formerly CRV431)

b)
a further payment of US$1,000,000
on first instance of net sales of an approved drug product containing Rencofilstat (a “Licensed Product”) exceeding
US$350,000,000; and

c)
a further payment of US$3,000,000
on first instance of net sales of a Licensed Product exceeding US$750,000,000.

did not recognize any contingent consideration given the high uncertainty of achieving these milestones.

On
February 25, 2026, we entered into an intellectual property license agreement with Cirna Diagnostics, LLC (“Cirna”)
pursuant to which we licensed certain liver disease diagnostic assets from Cirna. We will pay an upfront payment of $50,000 as well as
certain patent expenses, up to $2,350,000 in milestone payments, up to $4,500,000 in sales milestone payments and a royalty payment on
net sales in the low single digits.

Sales
and Marketing

currently do not have any commercialization or sales and marketing capabilities, and currently have no plans to invest in or build such
capabilities internally.

Manufacturing

do not own or operate any facilities in which we can formulate and manufacture our product candidates.

Pharmaceutical
Pricing and Reimbursement

In
the U.S. and most foreign markets, any revenue associated with the sale of our product candidate, if approved for sale, will depend largely
upon the availability of reimbursement from third-party payers. Third-party payers include various government health authorities such
as The Centers for Medicare and Medicaid Services (“CMS”), which administers Medicare and Medicaid in the U.S., managed-care
providers, private health insurers and other organizations. Third-party payers are increasingly challenging the price and examining the
cost-effectiveness of medical products and services, including pharmaceuticals. In addition, significant uncertainty exists as to the
reimbursement status of newly approved pharmaceutical products. Our products may ultimately not be considered cost-effective, and adequate
third-party reimbursement may not be available to enable us to maintain price levels sufficient to support a profitable operation or
generate an appropriate return on our investment in product development.

U.S. and foreign governments periodically propose and pass legislation designed to reduce the cost of healthcare and pharmaceutical products.
Accordingly, legislation and regulations affecting the pricing of pharmaceuticals may change before our product candidate is ever approved
for sale. In addition, the adoption of new legislation could further limit reimbursement for pharmaceuticals. Further, an increasing
emphasis on managed care in the U.S. has and will continue to increase the pressure on pharmaceutical pricing. The marketability of our
products may suffer if the government and other third-party payers fail to provide adequate coverage and reimbursement rates for our
product candidate.

Regulatory
Matters

Overview

preclinical and clinical testing, manufacture, labeling, storage, distribution, promotion, sale, export, reporting and record-keeping
of drug products and product candidates are subject to extensive regulation by numerous governmental authorities in the U.S., principally
the FDA and corresponding state agencies, and regulatory agencies in foreign countries.

Non-compliance
with applicable regulatory requirements can result in, among other things, total or partial suspension of the clinical development of
a product candidate, manufacturing and marketing, failure of the FDA or similar regulatory agency in other countries to grant marketing
approval, withdrawal of marketing approvals, fines, injunctions, seizure of products and criminal prosecution.

Government
Regulation

design, development, manufacture, testing and sale of our products in the U.S. are subject to regulation by numerous governmental authorities,
principally the FDA, and corresponding state and local regulatory agencies.

FDA
Regulation

Medical
Devices

Generally,
the products we develop must be cleared by the FDA before they are marketed in the United States. Before and after approval, authorization,
or clearance in the United States, our products are subject to extensive regulation by the FDA, as well as by other regulatory bodies.
FDA regulations govern, among other things, the development, testing, manufacturing, labeling, safety, storage, recordkeeping, market
clearance, authorization or approval, advertising and promotion, import and export, marketing and sales, and distribution of medical
devices, including IVDs. IVDs are a type of medical device and include reagents and instruments used in the diagnosis or detection of
diseases, conditions or infections, including, without limitation, the presence of certain chemicals or other biomarkers. Predictive,
prognostic and screening tests can also be IVDs.

In
the United States, medical devices are subject to varying degrees of regulatory control and are classified in one of three classes depending
on the extent of controls the FDA determines are necessary to reasonably ensure their safety and effectiveness:

●
Class
I: general controls, such as labeling and adherence to quality system regulations;

●

Class
II: special controls, premarket notification (often referred to as a 510(k)), specific controls such as performance standards,
patient registries, post-market surveillance, additional controls such as labeling and adherence to quality system regulations;
and

●
Class
III: special controls and requires a premarket approval (“PMA”).

FDA
Premarket Clearance and Approval Requirements

Unless
an exemption applies, each medical device commercially distributed in the United States requires either FDA clearance of a 510(k) premarket
notification, approval of a de novo application, or approval of a premarket approval (PMA).

While
most Class I devices are exempt from the 510(k) premarket notification requirement, manufacturers of most Class II devices are required
to submit to the FDA a premarket notification under Section 510(k) of the FDCA requesting permission to commercially distribute the device.
The FDA’s permission to commercially distribute a device subject to a 510(k) premarket notification is generally known as 510(k)
clearance. Devices deemed by the FDA to pose the greatest risks, such as life sustaining, life supporting or some implantable devices,
or devices that have a new intended use, or use advanced technology that is not substantially equivalent to that of a legally marketed
device, are placed in Class III, requiring approval of a PMA. Some pre-amendment devices are unclassified, but are subject to FDA’s
premarket notification and clearance process in order to be commercially distributed. Our initial product is a Class II device subject
to 510(k) clearance.

510(k)
Clearance Marketing Pathway

510(k)
clearance, a company must submit to the FDA a premarket notification submission demonstrating that the proposed device is “substantially
equivalent” to a predicate device already on the market. A predicate device is a legally marketed device that is not subject to
PMA, i.e., a device that was legally marketed prior to May 28, 1976 (pre-amendments device) and for which a PMA is not required, a device
that has been reclassified from Class III to Class II or I, or a device that was found substantially equivalent through the 510(k) process.
The FDA’s 510(k) clearance process usually takes from three to twelve months, but often takes longer. The FDA may require additional
information, including clinical data, to make a determination regarding substantial equivalence. In addition, the FDA collects user fees
for certain medical device submissions and annual fees for medical device establishments.

After
a device receives 510(k) marketing clearance, any modification that could significantly affect its safety or effectiveness, or that would
constitute a major change or modification in its intended use, will require a new 510(k) clearance or, depending on the modification,
PMA approval. The FDA requires each manufacturer to determine whether the proposed change requires submission of a 510(k) or a PMA in
the first instance, but the FDA can review any such decision and disagree with a manufacturer’s determination. If the FDA disagrees
with a manufacturer’s determination, the FDA can require the manufacturer to cease marketing and/or request the recall of the modified
device until 510(k) marketing clearance or PMA approval is obtained. Also, in these circumstances, the manufacturer may be subject to
significant regulatory fines or penalties.

De
Novo Classification

Devices
of a new type that FDA has not previously classified based on risk are automatically classified into Class III by operation of section
513(f)(1) of the FDCA, regardless of the level of risk they pose. To avoid requiring PMA review of low- to moderate-risk devices classified
in Class III by operation of law, Congress enacted section 513(f)(2) of the FDCA. This provision allows FDA to classify a low- to moderate-risk
device not previously classified into Class I or II. After de novo authorization, an authorized device may be used as a predicate for
future devices going through the 510(k) process.

Clinical
Trials

Clinical
trials are often required for a de novo authorization. All clinical investigations of devices to determine safety and effectiveness must
be conducted in accordance with the FDA’s IDE regulations which govern investigational device labeling, prohibit promotion of the
investigational device, and specify an array of recordkeeping, reporting and monitoring responsibilities of study sponsors and study
investigators. If the device presents a “significant risk,” to human health, as defined by the FDA, the FDA requires the
device sponsor to submit an IDE application to the FDA, which must become effective prior to commencing human clinical trials. A significant
risk device is one that presents a potential for serious risk to the health, safety or welfare of a patient and either is implanted,
used in supporting or sustaining human life, substantially important in diagnosing, curing, mitigating or treating disease or otherwise
preventing impairment of human health, or otherwise presents a potential for serious risk to a subject. An IDE application must be supported
by appropriate data, such as animal and laboratory test results, showing that it is safe to test the device in humans and that the testing
protocol is scientifically sound. The IDE will automatically become effective 30 days after receipt by the FDA unless the FDA notifies
the company that the investigation may not begin. If the FDA determines that there are deficiencies or other concerns with an IDE for
which it requires modification, the FDA may permit a clinical trial to proceed under a conditional approval.

In
addition, the study must be approved by, and conducted under the oversight of, an Institutional Review Board (IRB) for each clinical
site. The IRB is responsible for the initial and continuing review of the IDE study and may pose additional requirements for the conduct
of the study. If an IDE application is approved by the FDA and one or more IRBs, human clinical trials may begin at a specific number
of investigational sites with a specific number of patients, as approved by the FDA. If the device presents a non-significant risk to
the patient, a sponsor may begin the clinical trial after obtaining approval for the trial by one or more IRBs without separate approval
from the FDA, but must still follow abbreviated IDE requirements, such as monitoring the investigation, ensuring that the investigators
obtain informed consent, and labeling and record-keeping requirements. Acceptance of an IDE application for review does not guarantee
that the FDA will allow the IDE to become effective and, if it does become effective, the FDA may or may not determine that the data
derived from the trials support the safety and effectiveness of the device or warrant the continuation of clinical trials. An IDE supplement
must be submitted to, and approved by, the FDA before a sponsor or investigator may make a change to the investigational plan that may
affect its scientific soundness, study plan or the rights, safety or welfare of human subjects.

During
a study, the sponsor is required to comply with the applicable FDA requirements, including, for example, trial monitoring, selecting
clinical investigators and providing them with the investigational plan, ensuring IRB review, adverse event reporting, record keeping
and prohibitions on the promotion of investigational devices or on making safety or effectiveness claims for them. The clinical investigators
in the clinical study are also subject to FDA regulations and must obtain patient informed consent, rigorously follow the investigational
plan and study protocol, control the disposition of the investigational device, and comply with all reporting and recordkeeping requirements.
Additionally, after a trial begins, we, the FDA or the IRB could suspend or terminate a clinical trial at any time for various reasons,
including a belief that the risks to study subjects outweigh the anticipated benefits.

Sponsors
of applicable clinical trials of devices also are required to register with www.clinicaltrials.gov, a public database of clinical trial
information. Information related to the device, patient population, phase of investigation, study sites and investigators and other aspects
of the clinical trial is made public as part of the registration. Although the FDA’s Quality System Regulation (QSR) does not fully
apply to investigational devices, the requirement for controls on design and development does apply.

Post-market
Regulation

After
a device is cleared or approved for marketing, numerous and pervasive regulatory requirements continue to apply. These include:

●
establishment
registration and device listing with the FDA;

●

QSR
requirements, which require manufacturers, including third-party manufacturers, to follow stringent design, testing, control,
documentation and other quality assurance procedures during all aspects of the design and manufacturing process;

●

labeling
regulations and FDA prohibitions against the promotion of investigational products, or the promotion of “off-label” uses
of cleared or approved products;

●

requirements
related to promotional activities;

●

clearance
or approval of product modifications to 510(k)-cleared devices that could significantly affect safety or effectiveness or that would
constitute a major change in intended use of one of our cleared devices, or approval of certain modifications to PMA-approved devices;

●

medical
device reporting regulations, which require that a manufacturer report to the FDA if a device it markets may have caused or
contributed to a death or serious injury, or has malfunctioned and the device or a similar device that it markets would be likely to
cause or contribute to a death or serious injury, if the malfunction were to recur;

●

correction,
removal and recall reporting regulations, which require that manufacturers report to the FDA field corrections and product recalls
or removals if undertaken to reduce a risk to health posed by the device or to remedy a violation of the FDCA that may present a
risk to health;

●

the
FDA’s recall authority, whereby the agency can order device manufacturers to recall from the market a product that is in
violation of governing laws and regulations; and

●

post-market
surveillance activities and regulations, which apply when deemed by the FDA to be necessary to protect the public health or to
provide additional safety and effectiveness data for the device.

Once
we have a commercialized product, our manufacturing processes will be required to comply with the applicable portions of the QSR, which
cover the methods and the facilities and controls for the design, manufacture, testing, production, processes, controls, quality assurance,
labeling, packaging, distribution, installation and servicing of finished devices intended for human use. The QSR also requires, among
other things, maintenance of a device master file, device history file, and complaint files. As a manufacturer, we are subject to periodic
scheduled or unscheduled inspections by the FDA. Our failure to maintain compliance with the QSR requirements could result in the shut-down
of, or restrictions on, our manufacturing operations and the recall or seizure of our products, which would have a material adverse effect
on our business. The discovery of previously unknown problems with any of our products, including unanticipated adverse events or adverse
events of increasing severity or frequency, whether resulting from the use of the device within the scope of its clearance or off-label
by a physician in the practice of medicine, could result in restrictions on the device, including the removal of the product from the
market or voluntary or mandatory device recalls.

FDA has broad regulatory compliance and enforcement powers. If the FDA determines that we failed to comply with applicable regulatory
requirements, it can take a variety of compliance or enforcement actions, which may result in any of the following sanctions:

●
untitled
letters, warning letters, fines, injunctions, consent decrees and civil penalties;

●
unanticipated
expenditures to address or defend such actions;

●
customer
notifications or repair, replacement, refunds, recall, detention or seizure of our products;

●
operating
restrictions, partial suspension or total shutdown of production;

●
refusing
or delaying our requests for regulatory approvals or clearances of new products or modified products;

●
refusal
to grant export approval for our products; or

●
criminal
prosecution.

Federal
and State Fraud and Abuse Laws

are subject to federal fraud and abuse laws such as the federal Anti-Kickback Statute (AKS), the federal prohibition against physician
self-referral (Stark Law), the Eliminating Kickbacks in Recovery Act (EKRA), and the federal False Claims Act (FCA). We are also subject
to similar state and foreign fraud and abuse laws.

AKS (Social Security Act § 1128B(b)) prohibits knowingly and willfully offering, paying, soliciting, or receiving remuneration,
directly or indirectly, overtly or covertly, in cash or in kind, in return for or to induce such person to refer an individual, or to
purchase, lease, order, arrange for, or recommend purchasing, leasing or ordering, any item or service that may be reimbursable, in whole
or in part, under a federal healthcare program, such as Medicare or Medicaid. There are a number of statutory exceptions and regulatory
safe harbors to the AKS that provide protection from AKS liability to arrangements that fully satisfy the applicable requirements.

EKRA
(18 USC § 220) prohibits knowingly and willfully soliciting, receiving, offering or paying remuneration, directly or indirectly,
in return for the referral of a patient to, or in exchange for an individual using the services of certain entities, including laboratories,
if the services are covered by a health care benefit program. The term “health care benefit program” is broadly defined such
that EKRA extends to referrals reimbursed by both governmental and commercial third-party payers. EKRA includes a number of statutory
exceptions that provide protection from EKRA liability if the applicable requirements are met.

Stark Law (Social Security Act § 1877) generally prohibits, among other things, clinical laboratories and other so-called “designated
health services” entities from billing Medicare for any designated health services when the physician ordering the service, or
any member of such physician’s immediate family, has a financial relationship, such as a direct or indirect investment interest
in or compensation arrangement with the billing entity, unless the arrangement meets an exception to the prohibition. The Stark Law also
prohibits physicians from making such referrals to a designated health services entity. There are also similar state laws that apply
where Medicaid and/or commercial payers are billed.

FCA (31 USC § 3729) imposes penalties against individuals or entities for, among other things, knowingly presenting, or causing
to be presented, claims for payment to the government that are false or fraudulent, or knowingly making, using or causing to be made
or used a false record or statement material to such a false or fraudulent claim, or knowingly concealing or knowingly and improperly
avoiding, decreasing, or concealing an obligation to pay money to the federal government. This statute also permits a private individual
acting as a “qui tam” whistleblower to bring actions on behalf of the federal government alleging violations of the FCA and
to share in any monetary recovery. FCA liability is potentially significant in the healthcare industry because the statute provides for
treble damages and mandatory penalties per false claim or statement for penalties assessed.

Other
federal statutes pertaining to healthcare fraud and abuse include the civil monetary penalties statute, which prohibits, among other
things, the offer or payment of remuneration to a Medicaid or Medicare beneficiary that the offeror or payer knows or should know is
likely to influence the beneficiary to order or receive a reimbursable item or service from a particular provider, practitioner, or supplier,
and contracting with an individual or entity that the person knows or should know is excluded from participation in a federal health
care program. In addition, federal criminal statutes created by the Health Insurance Portability and Accountability Act (HIPAA) prohibit,
among other things, knowingly and willfully executing or attempting to execute a scheme to defraud any healthcare benefit program or
obtain by means of false or fraudulent pretenses, representations or promises any money or property owned by or under the control of
any healthcare benefit program in connection with the delivery of or payment for healthcare benefits, items or services.

In
addition to these federal laws, there are often similar state anti-kickback and false claims laws that typically apply to arrangements
involving reimbursement by a state-funded Medicaid or other health care program. Often, these laws closely follow the language of their
federal law counterparts, although they do not always have the same exceptions or safe harbors. In some states, these anti-kickback laws
apply with respect to all payers, including commercial payers.

A
number of states have enacted laws that require pharmaceutical and medical device companies to monitor and report payments, gifts and
other remuneration made to physicians and other healthcare providers, and, in some states, marketing expenditures. In addition, some
state statutes impose outright bans on certain manufacturer gifts to physicians or other health care professionals. Some of these laws,
referred to as “aggregate spend” or “gift” laws, carry substantial fines if they are violated.

Efforts
to ensure that our business arrangements with third parties will comply with applicable healthcare laws and regulations will involve
substantial costs and extensive annual trainings for all of our employees and contractors. If our operations are found to be in violation
of any of these laws or any other governmental regulations that may apply to us, we may be subject to significant civil, criminal and
administrative penalties, damages, fines, imprisonment, exclusion from participation in government-funded healthcare programs, such as
Medicare and Medicaid, disgorgement, contractual damages, reputational harm, diminished profits and future earnings, additional reporting
or oversight obligations if we become subject to a corporate integrity agreement or other agreement to resolve allegations of non-compliance
with the law, and the curtailment or restructuring of our operations, any of which could adversely affect our ability to operate our
business and our results of operations. If any of the physicians or other healthcare providers or entities with whom we do business is
found to be not in compliance with applicable laws, they may be subject to criminal, civil or administrative sanctions, including exclusions
from government-funded healthcare programs.

Anti-Corruption

FCPA and similar international bribery laws make it unlawful for persons or entities to make payments to foreign government officials
to assist in obtaining and maintaining business. Specifically, the anti-bribery provisions of the FCPA prohibit any offer, payment, promise
to pay, or authorizing the payment of money or anything of value to any person, while knowing that all or a portion of such money or
thing of value will be offered, given or promised, directly or indirectly, to a foreign official to do or omit to do an act in violation
of his or her duty, or to secure any improper advantage in order to assist in obtaining or retaining business for or with, or directing
business, to any person. In addition to the anti-bribery provisions of the FCPA, the statute also contains accounting requirements designed
to operate in tandem with the anti-bribery provisions. Covered companies are required to make and keep books and records that accurately
and fairly reflect the transactions of the company and devise and maintain an adequate system of internal accounting controls. With our
international operations through our third-party partnerships, we could incur significant fines and penalties, as well as criminal liability,
if we fail to comply with either the anti-bribery or accounting requirements of the FCPA, or similar international bribery laws. Even
an unsuccessful challenge of our compliance with these laws could cause us to incur adverse publicity and significant legal and related
costs.

Human
Capital

human capital objectives we focus on in managing our business include attracting, developing, and retaining key personnel. Our employees
are critical to the success of our organization, and we are committed to supporting our employees’ professional development. We
believe our management team has the experience necessary to effectively implement our growth strategy and continue to drive shareholder
value. We provide competitive compensation and benefits to attract and retain key personnel, while also providing a safe, inclusive and
respectful workplace. In December 2023, the board of directors approved a strategic restructuring plan to preserve capital by reducing
operating costs, which included a reduction in personnel in the first quarter of 2024.

As
of December 31, 2025, we had two employees.

Corporate
Information

were incorporated under the laws of the State of Delaware in May 2013. Our principal executive offices are located at 55 Madison Ave,
Suite 400- PMB #462, Morristown, New Jersey.

Available
Information

Our
annual report on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K, and other filings with the United States Securities
and Exchange Commission, or the SEC, and all amendments to these filings, are available, free of charge, on our website at www.Hepion.com
as soon as reasonably practicable following our filing of any of these reports with the SEC. You can also obtain copies free of charge
by contacting our Investor Relations department at our office address listed above. The public may read and copy any materials we file
with the SEC at the SEC’s Public Reference Room at 100 F Street NE, Room 1580, Washington, DC 20549. The public may obtain information
on the operation of the Public Reference Room by calling the SEC at 1-800-SEC-0330. The SEC maintains an Internet site that contains
reports, proxy, and information statements, and other information regarding issuers that file electronically with the SEC at www.sec.gov.
The information posted on or accessible through these websites are not incorporated into this filing.