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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 Jefferam1on Sep 07, 2018 2:57pm
62 Views
Post# 28581392

RE:RE:RE:ADvices from most-blocked, PoorOpinion!

RE:RE:RE:ADvices from most-blocked, PoorOpinion!https://www.antibethera.com/wordpress/wp-content/uploads/2018/08/Antibe-Phase-2B-Study-Review.pdf
Liver-related effects comparable to existing NSAIDs Blood levels of liver enzymes (including alanine transaminase (ALT) and aspartate transaminase (AST)) were measured on days 7 and 14 of treatment and at two-weeks posttreatment (day 28). Over the 14 day treatment course nonclinically significant treatment-related transient elevations in liver transaminases were observed in up to 7% of subjects receiving ATB-346 and up to 7% of subjects receiving naproxen. One subject receiving ATB-346 (0.8%) had clinically significant treatment-related transient transaminase elevations. At the two week post treatment follow up assessment 5.4% of the ATB-346-treated subjects had clinically significant, treatment-related, transient transaminase elevations that had resolved or were resolving. Cumulative data now obtained from three clinical trials in which ATB-346 has been dosed at 250 mg once daily for 10-14 days reveal a 4.7% overall incidence of clinically significant, transient liver transaminase increase; this can be contrasted to diclofenac, the most prescribed NSAID globally, where the incidence of clinically-significant liver transaminase elevations is up to 4%.
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