Galmed Reports Strong Bioavailability Results for Aramchol Meglumine in Phase 1 Study
Galmed Pharmaceuticals Ltd. has announced top-line results from its AM-001 Phase 1 bioavailability study of Aramchol meglumine. The study, which enrolled 30 healthy volunteers, compared the bioavailability of Aramchol meglumine granules to Aramchol free acid tablets. Findings indicate that Aramchol meglumine granules at doses of 400mg and 200mg demonstrated approximately 5-fold and 3-fold higher bioavailability, respectively, compared to the 300mg Aramchol free acid tablets. Based on these results, Galmed has identified a 400mg once-daily regimen as the optimal dose for future clinical trials. The company plans to advance Aramchol meglumine into Phase 2 oncology studies in the first half of 2026. Results from the AM-001 study have already been announced.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Galmed Pharmaceuticals Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: LN27422) on November 18, 2025, and is solely responsible for the information contained therein.
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