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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):
March 4, 2025
Adial Pharmaceuticals, Inc.
(Exact name of registrant as specified in charter)
Delaware |
|
001-38323 |
|
82-3074668 |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(IRS Employer
Identification No.) |
4870 Sadler Road, Ste 300
Glen Allen, VA 23060
(Address of principal executive offices and zip
code)
(804) 487-8196
(Registrant’s telephone number including
area code)
N/A
(Former name or former address, if changed
since last report)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of registrant under any of the following provisions (see General
Instruction A.2. below):
☐ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
☐ |
Soliciting material pursuant to Rule 14a-12(b) 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)) |
Securities registered pursuant to Section 12(b)
of the Act:
Title of each class |
|
Trading Symbols |
|
Name of each exchange on which registered |
Common Stock, par value $0.001 per share |
|
ADIL |
|
The Nasdaq Stock Market LLC
(Nasdaq Capital Market) |
Indicate by check mark whether the registrant
is an emerging growth company as defined in 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 checkmark
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 2.02 Results of Operations and Financial
Condition.
On March 4, 2025, Adial Pharmaceuticals, Inc.,
a Delaware corporation (the “Company”), issued a press release that included financial information for the fiscal year ended
December 31, 2024. A copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K.
The information in this Item 2.02 and in the press
release attached as Exhibit 99.1 to this Current Report on Form 8-K shall not be deemed to be “filed” for purposes of Section
18 of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section or Sections 11 and 12(a)(2)
of the Securities Act of 1933, as amended. The information contained in this Item 2.02 and in the press release attached as Exhibit 99.1
to this Current Report on Form 8-K shall not be incorporated by reference into any filing with the U.S. Securities and Exchange Commission
made by the Company, whether made before or after the date hereof, regardless of any general incorporation language in such filing.
Item 9.01 Financial Statements and Exhibits.
(d) Exhibits
The following
exhibits are furnished with this Current Report on Form 8-K:
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 hereunto duly authorized.
Dated: March 4, 2025 |
ADIAL PHARMACEUTICALS, INC. |
|
|
|
By: |
/s/ Cary J. Claiborne |
|
Name: |
Cary J. Claiborne |
|
Title: |
President and Chief Executive Officer |
2
Exhibit 99.1
Adial Pharmaceuticals
Reports 2024 Fiscal Year Financial Results
and Provides Business Update
Glen Allen, VA – March 4, 2025 –
Adial Pharmaceuticals, Inc. (NASDAQ: ADIL) (“Adial” or the “Company”), a clinical-stage biopharmaceutical
company focused on developing therapies for the treatment and prevention of addiction and related disorders, today provided a business
update and reported its financial results for the 2024 fiscal year ended December 31, 2024.
Key Highlights
| ● | Successful completion of AD04-103 pharmacokinetics
(PK) study of AD04, corroborating bioavailability, dose proportionality, no food effect, and safety profile consistent with the use of
Ondansetron. |
| ○ | Advancement towards pivotal Phase 3 trial design supportive of ongoing partnership discussions. |
| ● | FDA confirmation of proposed 505(b)(2) bridging strategy leveraging
the results from AD04-103—a relative bioavailability food-effect study—along with in vitro dissolution data demonstrating
equivalence between the reference product and the planned commercial formulation of AD04. |
| ○ | FDA positive response confirms that design of data package would meet the requirements necessary to allow
for the progression of AD04 into Phase 3 clinical trials. |
| ● | With FDA confirmation, Adial is commencing
manufacturing of clinical supplies for Phase 3 clinical program in 2025. |
| ● | Secured several foundational patents, strengthening
IP portfolio in support of commercialization of AD04, including: |
| ○ | New U.S. patent granted expanding coverage
of Adial’s genetic-based approach to treating and diagnosing Alcohol Use Disorder (AUD) and other drug dependencies. |
| ○ | New U.S. Patent granted covering genotype-specific treatment of opioid-related disorders. |
| ○ | New U.S. Patent granted for the treatment of alcohol and drug dependence based on expanded genotype
combinations. |
“We achieved meaningful milestones in 2024,
leading to positive feedback from the U.S. Food and Drug Administration (FDA) regarding our proposed 505(b)(2) bridging strategy and the
initiation of clinical supply manufacturing for our upcoming Phase 3 trial this year,” said Cary Claiborne, CEO of Adial Pharmaceuticals.
“A key achievement was the completion of our pharmacokinetics (PK) study evaluating AD04, our investigational drug for the treatment
of Alcohol Use Disorder (AUD). This study assessed the PK profile, bioavailability, and food effect of AD04 near-micro doses compared
to marketed Ondansetron in healthy volunteers. The findings enabled the FDA to confirm the bridging requirements for our 505(b)(2) registration
pathway and support our planned micro-dosing regimen for the upcoming registrational trials.”
“In addition to the key highlights mentioned,
we strengthened our regulatory strategy by partnering with Boudicca Dx to advance the development of our companion diagnostic genetic
test for AD04. Boudicca Dx, a global leader in precision medicine testing, has been instrumental in ensuring our test meets FDA technical
and clinical validation standards. This collaboration played an important role in our discussions with the FDA and further solidified
our regulatory pathway.”
“With these foundational steps in place,
we are well-positioned to initiate our Phase 3 clinical trials in 2025. Our focus remains on advancing AD04 as efficiently as possible
to provide a much-needed treatment option for individuals struggling with addiction,” concluded Mr. Claiborne.
Other Developments
Management
On November 5, 2024, Adial announced the appointment
of Vinay Shah as the Company’s Chief Financial Officer. Mr. Shah is an accomplished Chief Financial Officer with over 25 years of
experience in the pharmaceutical, biopharmaceutical, and healthcare sectors, specializing in financial strategy, investor relations, and
operational efficiency.
Intellectual Property
On February 19, 2025, Adial announced patent number
12,226,401 was issued on February 18, 2025, by the United States Patent and Trademark Office (USPTO). The patent covers claims that focus
on a method for identifying genetic markers in patients with alcohol or opioid-related disorders including the AC genotype of rs17614942
in the HTR3B gene and the AG genotype of rs1150226 in the HTR3A gene.
On February 12, 2025, Adial announced patent number
12,221,654 was issued on February 11, 2025, by the USPTO. This patent expands the covered methods of identifying patients with specific
genetic markers linked to substance use disorders and treating them with AD04. The treatment approach involves detecting the TT genotype
of rs1042173 in the serotonin transporter gene (SLC6A4) and administering AD04.
On December 3, 2024, Adial announced patent number
12,150,931 was issued on November 26, 2024, by the USPTO. The patent covers a broader range of genotype combinations identified by the
Company’s proprietary genetic diagnostic for targeted treatment of alcohol use disorder (AUD) with AD04. These genotype combinations
include the HTR3A, HTR3B, and SLC6A4 receptor sites.
Commendation
On October 15, 2024, Adial applauded the National
Institute on Alcohol Abuse and Alcoholism (NIAAA) for its newly updated definition of recovery. The new definition, outlined and emphasized
in NIAAA’s 2025 Professional Judgement Budget (PJB) as reported to the U.S. Congress following an original introduction in an NIAAA
PJB, emphasizes a broader, non-abstinence approach to recovery, which aligns directly with Adial’s AD04 program, which has the potential
to offer patients the flexibility of reducing drinking and, or abstinence.
Fiscal Year 2024 Financial Results
| ● | Cash and cash equivalents were $3.8 million as of December 31, 2024, compared to $2.8 million as of December
31, 2023. The Company believes that its existing cash and cash equivalents will fund its operating expenses into the second half of 2025
based on currently committed development plans. |
| ● | Research and development expenses increased by approximately $1.9 million (155%) during the year ended
December 31, 2024, compared to the year ended December 31, 2023. The key drivers of this increase were an increase of approximately $1.4
million of direct clinical trial expenses associated with the PK study initiated in 2024, and an increase of approximately $813 thousand
of chemistry, manufacturing, and controls (CMC) expenses, as stability testing took place to support the PK study in 2024, and drug product
manufacturing was initiated to support the upcoming Phase 3 clinical program. |
| ● | General and administrative expenses decreased by approximately $491 thousand (9%) during the year ended
December 31, 2024, compared to the year ended December 31, 2023. This decrease was the result of lower corporate legal expenses of approximately
$269 thousand and a decrease in compensation of approximately $215 thousand, including equity-based compensation of G&A personnel. |
| ● | Net Loss was $13.2 million for the year ended December 31, 2024, compared to a net loss of $5.1 million
for the year ended December 31, 2023. The increase in net loss was primarily driven by non-cash charges of $4.5 million for an inducement
expense and $0.6 million loss on our equity method investment along with increases in R&D spending offset by a decrease in G&A
spending. |
About Adial Pharmaceuticals, Inc.
Adial Pharmaceuticals is a clinical-stage biopharmaceutical
company focused on the development of therapies for the treatment and prevention of addiction and related disorders. The Company’s
lead investigational new drug product, AD04, is a genetically targeted, serotonin-3 receptor antagonist, therapeutic agent for the treatment
of Alcohol Use Disorder (AUD) in heavy drinking patients and was recently investigated in the Company’s ONWARD™ pivotal Phase
3 clinical trial for the potential treatment of AUD in subjects with certain target genotypes identified using the Company’s proprietary
companion diagnostic genetic test. ONWARD showed promising results in reducing heavy drinking in heavy drinking patients, and no overt
safety or tolerability concerns. AD04 is also believed to have the potential to treat other addictive disorders such as Opioid Use Disorder,
gambling, and obesity. Additional information is available at www.adial.com.
If you are interested in exploring partnership
opportunities with Adial, we invite you to reach out to us (BD@adialpharma.com) to discuss how our joint efforts can bring about positive
change to the millions of patients who are struggling with addiction.
Forward-Looking Statements
This communication contains certain “forward-looking
statements” within the meaning of the U.S. federal securities laws. Such statements are based upon various facts and derived utilizing
numerous important assumptions and are subject to known and unknown risks, uncertainties and other factors that may cause actual results,
performance or achievements to be materially different from any future results, performance or achievements expressed or implied by such
forward-looking statements. Statements preceded by, followed by or that otherwise include the words “believes,” “expects,”
“anticipates,” “intends,” “projects,” “estimates,” “plans” and similar expressions or
future or conditional verbs such as “will,” “should,” “would,” “may” and “could” are
generally forward-looking in nature and not historical facts, although not all forward-looking statements include the foregoing. The forward-looking
statements include statements regarding being well-positioned to initiate Phase 3 clinical trials in 2025, advancing AD04 as efficiently
as possible to provide a much-needed treatment option for individuals struggling with addiction, existing cash and cash equivalents funding
operating expenses into the second half of 2025 and the potential of AD04 to treat other addictive disorders such as opioid use disorder,
gambling, and obesity. Any forward-looking statements included herein reflect our current views, and they involve certain risks and uncertainties,
including, among others, our ability to pursue our regulatory strategy, our ability to advance ongoing partnering discussions, our ability
to obtain regulatory approvals for commercialization of product candidates or to comply with ongoing regulatory requirements, our ability
to develop strategic partnership opportunities and maintain collaborations, our ability to obtain or maintain the capital or grants necessary
to fund our research and development activities, our ability to complete clinical trials on time and achieve desired results and benefits
as expected, regulatory limitations relating to our ability to promote or commercialize our product candidates for specific indications,
acceptance of our product candidates in the marketplace and the successful development, marketing or sale of our products, our ability
to maintain our license agreements, the continued maintenance and growth of our patent estate and our ability to retain our key employees
or maintain our Nasdaq listing. These risks should not be construed as exhaustive and should be read together with the other cautionary
statement included in our Annual Report on Form 10-K for the year ended December 31, 2023, subsequent Quarterly Reports on Form 10-Q and
current reports on Form 8-K filed with the Securities and Exchange Commission. Any forward-looking statement speaks only as of the date
on which it was initially made. We undertake no obligation to publicly update or revise any forward-looking statement, whether as a result
of new information, future events, changed circumstances or otherwise, unless required by law.
Contact:
Crescendo Communications, LLC
David Waldman / Alexandra Schilt
Tel: 212-671-1020
Email: ADIL@crescendo-ir.com
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