Adial Pharmaceuticals, Inc. (NASDAQ: ADIL; ADILW)
(“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 second
quarter of 2022.
William Stilley, Adial’s Chief Executive
Officer, stated, “We recently reported successful results from the
ONWARD trial, our Phase 3 clinical study evaluating the efficacy,
safety and tolerability of AD04 in patients with Alcohol Use
Disorder (“AUD”) and selected polymorphisms in the serotonin
transporter and receptor genes. The results showed that AD04
achieved a statistically significant mean reduction in heavy
drinking days among the pre-specified group of “heavy drinkers”
(avg. <10 drinks per drinking day at baseline), which accounted
for approximately two-thirds of the trial population. We did not
achieve statistical significance among “very heavy drinkers” (avg.
≥10 drinks per drinking day at baseline) due to the high placebo
response among this particularly challenging patient population,
which resulted in us not achieving the primary efficacy analysis
among the combined population. Nevertheless, given the strength of
the data, especially the statistical significance among heavy
drinkers, as well as the safety and tolerability of AD04, we have
consulted with both key opinion leaders and our regulatory
advisors. Based on the feedback, we strongly believe there is a
clear path forward to regulatory submission, and we are more
encouraged than ever about the potential for
commercialization.”
Cary Claiborne, Chief Operating Officer of
Adial, further noted, “Moving forward, we are working diligently to
submit the ONWARD results to both the U.S. Food and Drug
Administration (“FDA”) and the European Medicines Authority
(“EMA”). Moreover, we are actively exploring potential partnership
opportunities in both the U.S. and Europe. Based on just the heavy
drinking population alone, which constitutes the majority of AUD
patients, we estimate the addressable U.S. market for AD04 to be in
the multi-billion dollar range. Overall, we are very pleased with
our progress and look forward to providing updates as additional
developments unfold.”
Other Recent Developments
Patents
Adial has been awarded key patents for AD04 in
the United States, European Union and other jurisdictions,
including its latest patent issued on June 7, 2022 that expands
coverage of a previously issued patent to include the measurement
of the genetic biomarkers for all of the targeted genotypes
utilizing our proprietary diagnostic test. This patent estate
provides protection through 2031 with expected extensions until
2036.
Purnovate
The Company continues to advance programs
developed using its adenosine platform, through its wholly-owned
subsidiary, Purnovate, Inc. During the quarter, the Company
announced research collaborations with leading adenosine experts to
advance research and development of its compounds based on positive
pre-clinical data. The Company announced research collaborations
with the Medical College of Wisconsin related to the treatment of
diabetes and non-alcoholic steatohepatitis (NASH), as well as UC
San Diego related to the treatment of inflammatory diseases,
including inflammatory bowel disease (IBD) and infectious diseases
where a large immune response (i.e., cytokine storm) plays a
significant role. The Company continues to advance its Purnovate
compounds towards first-in-human clinical trials and has commenced
cGMP manufacturing and IND enabling toxicology studies.
Second Quarter 2022 Financial
Results
- Cash Position:
As of June 30,2022, cash and cash equivalents were $9.2 million as
compared to $6.1 million as of December 31, 2021, which the Company
believes provides sufficient runway to advance ongoing regulatory
and partnering activities related to AD04, as well as advancement
of its Purnovate platform.
- Research and
Development expenses decreased by $1.1 million to $1.2 million for
second quarter of 2022, as compared to $2.3 million in the second
quarter of 2021. The decrease was driven by lower costs related to
the ONWARD Phase 3 trial as clinical activities were substantially
complete by the second quarter of 2022.
- General and
Administration expenses increased by $0.5 million to $2.6 million
for the second quarter of 2022 as compared to $2.1 million in the
second quarter of 2021, with $0.3 million of the increase related
to non-cash items. General and administrative expenses held
generally steady in the six months ended June 30, 2022, when
compared to the six months ended June 30, 2021.
- Net Loss was
$3.8 million for the second quarter of 2022 as compared to a net
loss of $4.4 million in the second quarter of 2021. Net loss per
share for the second quarter of 2022 was $0.16, compared to a net
loss of $0.25 per share in the second quarter of 2021.
About Adial Pharmaceuticals,
Inc.
Adial Pharmaceuticals is a clinical-stage
biopharmaceutical company focused on the development of treatments
for addictions. 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 (estimated to be approximately one-third of the
AUD population) 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. The Company is also developing
adenosine analogs for the treatment of pain and other disorders.
Additional information is available at www.adial.com.
About Purnovate, Inc.
Purnovate, Inc., a wholly owned subsidiary of
Adial Pharmaceuticals, Inc., is a pharmaceutical development and
chemistry company focused on inventing and developing selective,
potent, stable, and soluble drug candidates targeting the adenosine
receptors to treat diseases and disorders such as pain, asthma,
cancer, diabetes, non-alcoholic steatohepatitis (NASH), and
inflammatory diseases and disorders such as burn/wound healing,
inflammatory bowel disorder and infectious disease.
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 there being a clear path forward to regulatory
submission, being more encouraged than ever about the potential for
commercialization, submitting the ONWARD results to both the U.S.
Food and Drug Administration (“FDA”) and the European Medicines
Authority (“EMA”),exploring potential partnership opportunities in
both the U.S. and Europe, the addressable U.S. market for AD04
being in the multi-billion dollar range based on just the heavy
drinking population alone, which constitutes the majority of AUD
patients, providing updates as additional developments unfold,
continuing to advance programs developed using Purnovate’s
adenosine platform, Purnovate, Inc. continuing to advance its
compounds towards first-in-human clinical trials and cash and cash
equivalents providing sufficient runway to advance ongoing
regulatory and partnering activities related to AD04, as well as
advancement of Purnovate’s platform. Any forward-looking statements
included herein reflect our current views, and they involve certain
risks and uncertainties, including, among others, our ability to
complete clinical trials on time and achieve desired results and
benefits as expected, our ability to obtain regulatory approvals
for commercialization of product candidates or to comply with
ongoing regulatory requirements, 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, our ability
to establish and maintain collaborations, our ability to obtain or
maintain the capital or grants necessary to fund our research and
development activities, our cash runway being sufficient to advance
ongoing regulatory and partnering activities related to AD04, as
well as advancement of Purnovate’s platform, 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, 2021,
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 / Natalya
Rudman Tel:
212-671-1021 Email:
adil@crescendo-ir.com
Adial Pharmaceuticals (NASDAQ:ADILW)
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