Artelo Biosciences Announces Acceptance of ART26.12 into the National Institutes of Health’s “Preclinical Screening Platform for Pain” Program
05 Novembro 2024 - 10:30AM
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 ART26.12, the Company’s lead clinical FABP
inhibitor, has been accepted into the NIH Helping to End Addiction
Long Term (HEAL) Initiative’s Preclinical Screening Platform for
Pain (PSPP).
The HEAL Initiative is an NIH-wide effort to accelerate
scientific solutions to the overdose epidemic, including opioid and
stimulant use disorders, and the crisis of pain. Launched in April
2018, the initiative is focused on improving prevention and
treatment strategies for opioid misuse and addiction, and enhancing
pain management. For more information, visit:
https://heal.nih.gov.
The PSPP program, part of the NIH HEAL Initiative, evaluates
non-opioid assets in a battery of established preclinical pain
models. The PSPP program accepts small molecules,
biologics, devices, or natural products for evaluation,
from researchers in academia and industry worldwide. For more
information, visit:
https://heal.nih.gov/research/preclinical-translational/screening-platform.
The content of this press release is solely the responsibility
of the authors and does not necessarily represent the official
views of the NIH.
“Access to the PSPP program will advance our understanding and
development of ART26.12,” commented Saoirse O’Sullivan, PhD, Vice
President Translational Science at Artelo Biosciences. “We are most
gratified to be recognized and accepted into the PSPP Program.”
Artelo previously announced that the U.S. Food and Drug
Administration (FDA) notified the Company that the first-in-human
study with ART26.12 may proceed. Initial study results are expected
during first half of 2025.
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
initial clinical development 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, dermatologic conditions, and
anxiety disorders. The Company recently received FDA clearance
of its Investigational New Drug application for ART26.12, for the
treatment of CIPN.
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.
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,
dermatologic conditions, 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. More information is available at
www.artelobio.com and Twitter: @ArteloBio.
Forward Looking Statements
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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
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investors are cautioned not to place undue reliance on such
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Investor Relations Contact:Crescendo
Communications, LLCTel: 212-671-1020Email:
ARTL@crescendo-ir.com
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