Galmed reports 500% bioavailability boost for oral aramchol formulation
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Galmed Announces Results from First-in-Man Pharmacokinetics Study of Oral Formulation of Aramchol Meglumine (AM); 400mg AM Increases Bioavailability by ~500% in Comparison to Aramchol Free Acid (AA) 3
May 14, 2026 7:30 AM EDTResults from Study AM-001 mark a pivotal advance through the transition to a once daily lower 400mg dose of AM enabling:
Production of GMP clinical batch for Galmed's upcoming clinical trialsSolidification and prolongation of Aramchol's IP protectionPotential reduction in drug CoGs by ~50%Improvement in patients' convenience and compliance upon potential commercializationRAMAT-GAN, Israel, May 14, 2026 /PRNewswire/ --Â Galmed Pharmaceuticals Ltd. (NASDAQ:... More
