Antibe Therapeutics Announces Additional Validation Data on ATB-346
17 Abril 2015 - 8:45AM
Business Wire
Antibe Therapeutics Inc. (“Antibe” or the “Company”) (TSXV:ATE)
announced today the results of additional testing of the in vivo
activity of its lead anti-inflammatory drug, ATB-346.
The results support the Company's earlier communication that
ATB-346 may be effective at much lower doses than previously
expected, and that once daily dosing may be effective. Together,
over 600 blood samples from its Phase 1 human clinical trial were
independently analysed to assess the ability of ATB-346, at doses
ranging from 25 to 1000 mg, to inhibit the enzyme "cyclooxygenase"
(COX). The reduction of pain and inflammation by non-steroidal
anti-inflammatory drugs (NSAIDs) is attributed to their ability to
inhibit COX activity.
Substantial inhibition of COX was observed at doses of ATB-346
as low as 75 mg, and the inhibition was maintained for 24
hours.
The Company continues to conduct validation studies, and will
report to the market as they proceed.
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 lead drug ATB-346 targets the global need for a
safer non-steroidal anti-inflammatory drug (NSAID) for chronic pain
and inflammation. ATB-352, the second drug in Antibe’s pipeline,
targets the urgent global need for a safer analgesic for severe
acute pain.
www.antibethera.com
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.
Important Note on Forward Looking Statements
Antibe Therapeutics Inc.Dan Legault, 416-473-4095Chief Executive
Officerdan.legault@antibethera.com
Antibe Therapeutics (TSXV:ATE)
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