Artelo Biosciences,
Inc.
(Nasdaq: ARTL), a
clinical-stage pharmaceutical company focused on modulating
lipid-signaling pathways to develop treatments for people living
with cancer, pain, dermatologic and neurological conditions, today
announced that George Warren, Ph.D., Principal Scientist at Artelo,
Myles Osborn, Medicinal Chemist at Artelo, and Matthew Jones, Ph.D.
candidate from the Laviolette laboratory at the University of
Western Ontario, Canada, each presented results from research
studies demonstrating the broad therapeutic potential of Fatty Acid
Binding Protein 5 (FABP5) inhibition at the 34th Annual
International Cannabinoid Research Society (ICRS) Symposium. The
ICRS Symposium is being held June 30 – July 5, 2024 in Salamanca,
Spain.
Targeting FABP5, a promising new approach to treat cancer, was
featured in the presentation “Efficacy of ART26.12, a Novel Fatty
Acid Binding Protein 5 Inhibitor, in an Orthotopic HCT-116-LUC
Human Colon Cancer Model.” Myles Osborn discussed novel preclinical
data showing a direct anti-tumoral effect of oral treatment with
ART26.12. These data are also supportive of Artelo’s planned
development of ART26.12 in chemotherapy-induced peripheral
neuropathy, where ART26.12 may be able to aid in treatment of the
underlying cancer, in addition to the debilitating effects of
painful neuropathies.
Beyond development for pain and cancer, ART26.12 has also shown
the potential for therapeutic activity in dermatologic conditions.
FABP5 was first identified in psoriatic lesions and there is
evidence to suggest that upregulation of FABP5 contributes to the
pathology of psoriasis. Regarding the data in his presentation, “A
Novel Fatty Acid-binding Protein 5 Inhibitor Shows Efficacy in
Preclinical Models of Psoriasis,” George Warren, Ph.D. commented,
“We are pleased to share novel data showing that our lead FABP5
inhibitor, ART26.12, demonstrated compelling data in preclinical
models of psoriasis. In this study, ART26.12 reduced the severity
of histopathological markers of skin damage and reduced markers of
oxidative stress, chemokines, cytokines, and keratinocyte
proliferation, and increased antimicrobial peptides. Results were
obtained using a standard imiquimod mouse model, which demonstrated
ART26.12 had similar levels of activity as Sotyktu
(deucravacitinib), an oral tyrosine kinase 2 inhibitor approved by
the U.S. Food and Drug Administration in 2022 to treat psoriasis.
Sales of Sotyktu may reach $4 billion by the end of the decade,
according to Bristol Myers Squibb.”
In addition to ART26.12, another one of Artelo’s FABP5
inhibitors was featured in a presentation entitled, “Inhibition of
Fatty Acid Binding Protein 5 Prevents Stress-induced Anxiety and
Depressive-Like Behavioral Symptoms and Reverses Stress-induced
Inhibition of Hippocampal Neurogenesis” where Matthew Jones
discussed new results from ongoing studies being conducted at the
laboratory of Dr. Steven Laviolette. The data showed that Artelo’s
FABP5 inhibitor SBFI103 improved depressive-like behaviors in rats
after chronic unpredictable stress, associated with increases in
markers of neurogenesis, a critical process in which newly formed
neural cells are added to the existing neural network. “This new
data supports our laboratory’s earlier work showing SBFI103 reduces
anxiety and increased fear memory extinction. These studies
implicate a role for the cannabinoid receptor 2 mediating the
effects of FABP5 inhibition in the brain,” concluded Jones.
“We are pleased to share the expanding evidence for the
potential utility of inhibiting FABP5,” stated Gregory D. Gorgas,
President and Chief Executive Officer of Artelo. “These important
scientific advances show that lipid modulation is a promising
therapeutic strategy across multiple diseases where overactivity of
the lipidome contributes to the pathology of the disease or where
modulation of the lipidome leads to increased levels of analgesic
and anxiolytic lipids. We are grateful for the opportunity to share
our data and why we believe development of FABP5 inhibitors from
our extensive library could have significant impact for a wide
range of diseases. We expect to report on first-in-human trials
with ART26.12 next year.”
About ART26.12Fatty Acid Binding Proteins
(FABPs) are a family of intracellular proteins that chaperone
lipids including endocannabinoids and fatty acids. FABP is
overexpressed and associated with abnormal lipid signaling in a
number of pathologies. ART26.12, Artelo’s lead FABP inhibitor, is a
potent and selective inhibitor of FABP5 being developed as a novel,
peripherally acting, non-opioid, non-steroidal analgesic, with an
initial clinical study planned for chemotherapy-induced peripheral
neuropathy (CIPN). Beyond ART26.12, Artelo’s extensive library of
small molecule inhibitors of FABPs have shown therapeutic promise
for the treatment of certain cancers, neuropathic and nociceptive
pain, and anxiety disorders.
About the International Cannabinoid Research
SocietyThe International Cannabinoid Research
Society (ICRS) is the premier global scientific association
with more than 650 international members from 40 countries, all
active researchers in the field of endogenous, plant-derived, and
synthetic cannabinoids and related bioactive lipids. In addition to
acting as a source for impartial information on cannabis and the
cannabinoids, the main role of the ICRS is to provide an open forum
for researchers to meet and discuss their research. The ICRS
Symposium is being held June 30 – July 5, 2024 in
Salamanca, Spain.
About Artelo Biosciences Artelo Biosciences,
Inc. is a clinical stage pharmaceutical company dedicated to
the development and commercialization of proprietary therapeutics
that modulate lipid-signaling pathways including the
endocannabinoid system. Artelo is advancing a portfolio of broadly
applicable product candidates designed to address significant unmet
needs in multiple diseases and conditions, including anorexia,
cancer, anxiety, pain, and inflammation. Led by proven
biopharmaceutical executives collaborating with highly respected
researchers and technology experts, the company applies leading
edge scientific, regulatory, and commercial discipline to develop
high-impact therapies. For more information and to view available
publications, please visit https://artelobio.com/science/.
Forward Looking StatementsThis press release
contains certain forward-looking statements within the meaning of
Section 27A of the Securities Act of 1933 and Section 21E of the
Securities Exchange Act of 1934 and Private Securities Litigation
Reform Act, as amended, including those relating to the Company’s
product development, clinical and regulatory timelines, market
opportunity, competitive position, possible or assumed future
results of operations, business strategies, potential growth
opportunities and other statement that are predictive in nature.
These forward-looking statements are based on current expectations,
estimates, forecasts and projections about the industry and markets
in which we operate and management’s current beliefs and
assumptions. These statements may be identified by the use of
forward-looking expressions, including, but not limited to,
“expect,” “anticipate,” “intend,” “plan,” “believe,” “estimate,”
“potential,” “predict,” “project,” “should,” “would” and similar
expressions and the negatives of those terms. These statements
relate to future events or our financial performance and involve
known and unknown risks, uncertainties, and other factors which may
cause actual results, performance or achievements to be materially
different from any future results, performance or achievements
expressed or implied by the forward-looking statements. Such
factors include those set forth in the Company’s filings with the
Securities and Exchange Commission, including our ability to raise
additional capital in the future. Prospective investors are
cautioned not to place undue reliance on such forward-looking
statements, which speak only as of the date of this press release.
The Company undertakes no obligation to publicly update any
forward-looking statement, whether as a result of new information,
future events or otherwise, except to the extent required by
applicable securities laws.
Investor Relations Contact:Crescendo
Communications, LLCTel:
212-671-1020Email: ARTL@crescendo-ir.com
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