Antibe Therapeutics Provides Update on Its Acute Pain Drug ATB-352
November 25 2014 - 7:30AM
Business Wire
Antibe Therapeutics Inc. (“Antibe” or the “Corporation”) (TSXV:
ATE; OTCQX: ATBPF) is pleased to report results from animal
proof-of-concept studies on ATB-352, which is the second drug in
the Company’s pipeline, as described in the CEO Letter of April
2014. These studies have demonstrated that ATB-352 potently
inhibits the production of pain-signalling chemicals
(prostaglandins) in rats, but does not produce significant
ulceration in the stomach or intestine, even at very high doses. In
the same study, administration of the painkiller ketoprofen caused
severe and extensive intestinal ulceration and bleeding.
“ATB-352 has a novel mechanism of action,” said Antibe’s Chief
Science Officer, Dr. John Wallace. “The small amounts of hydrogen
sulfide that are released from this drug exert a potent protective
effect in the stomach and intestine. This drug was designed to
address a substantial unmet medical need, and a market exceeding $2
billion annually.”
ATB-352 is a potent pain-killer intended for use in the
short-term treatment of conditions characterized by severe pain,
including that associated with herniated discs, gout, ankylosing
spondylitis, migraines, traumatic injuries, muscle aches,
post-surgical pain, toothache and menstrual cramps. Dan Legault,
Antibe’s CEO remarked, “For many patients, there are only two
viable options for treatment of severe pain: traditional
non-steroidal anti-inflammatory drugs (NSAIDs), which can cause
severe gastrointestinal bleeding, and opiates, which carry the
risks of addiction and abuse. ATB-352 is intended to provide an
important third option to this large group of patients.”
About Antibe Therapeutics Inc.
Antibe develops safer medicines for pain and inflammation.
Antibe’s technology involves linking a hydrogen sulfide-releasing
molecule to an existing drug to produce a patented, improved
medicine. Antibe’s ATB-346 targets the global need for safer
non-steroidal anti-inflammatory drugs (NSAIDs).
Neither the TSX Venture Exchange nor its Regulation Services
Provider (as that term is defined in the policies of the TSX
Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release.
Antibe Therapeutics Inc.Dan Legault, 416-473 4095Chief Executive
Officerdan.legault@antibethera.comwww.antibethera.com
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