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Antibe Therapeutics Inc(Pre-Merger) ATBPF

Antibe Therapeutics Inc. is a clinical-stage biotechnology company. The Company is leveraging its hydrogen sulfide (H2S) platform to develop therapies to target inflammation arising from a range of medical conditions. The Company’s pipeline includes assets that seek to overcome the gastrointestinal ulcers and bleeding associated with nonsteroidal anti-inflammatory drugs (NSAIDs). Its lead drug, otenaproxesul, is in clinical development as an alternative to opioids and NSAIDs for acute pain. Its second pipeline drug, ATB-352, is being developed for a specialized pain indication. The Company also focuses on inflammatory bowel disease (IBD). Otenaproxesul combines a moiety that releases hydrogen sulfide with naproxen, a non-steroidal, anti-inflammatory drug. ATB-352 is an H2S-releasing derivative of ketoprofen, a potent NSAID commonly prescribed for acute pain. Its IBD candidates are being designed to maintain the efficacy, safety, and pharmacokinetic properties of ATB-429.


GREY:ATBPF - Post by User

Comment by MrMugsyon Mar 26, 2021 10:05am
270 Views
Post# 32885450

RE:RE:RE:Quick update: Pfizer’s tanezumab voted down!

RE:RE:RE:Quick update: Pfizer’s tanezumab voted down!
TriumphSpitSix wrote: This gives us good goal posts to aim for.

Our Ph.3 needs to provide "convincing evidence of a superior efficacy" of OTEN over NSAIDs (easy) and any dose-related adverse events need to plateau (or better, trail off) by the end of the study. (Harder since we only have safety data out to 2-3 weeks tops and Ph. 3 is 12 weeks of dosing.)  

This supports my prior suggestion that Antibe could reduce the dosage down into the sub-100mg level and still demonstrate superiority to NSAIDS (Naproxen specifically) and more importantly, significantly reduce the possibility of adverse GI or hepatic effects over the much longer Ph. 3 dosing period than we currently have data for.

Better safe (and still obviously better than other NSAIDS) than sorry.


Triumph ... superiority in safety (that's the key).
On the efficacy side (pain and inflammation) - we are not aiming for superiority - want to be "as good" as the other alternatives, with less NSAID (active ingredient).

I think we mean the same - just wanted to clarify.
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