Anavex withdraws EU marketing application for Alzheimer's drug

Go back to Anavex withdraws EU marketing application for Alzheimer's drug

Anavex Life Sciences Provides Comprehensive Regulatory Update

March 30, 2026 7:30 AM EDT

Dialogue continues with European Medicines Agency (EMA) to advance the development program of oral blarcamesine in early Alzheimers disease

Additional data submitted to the U.S. FDA with the objective to discuss potential pathways towards a New Drug Application (NDA) for the treatment of early Alzheimers disease

Additionally, Anavex has engaged in discussions with EU regulators regarding blarcamesine for Parkinsons disease and rare diseases, including Rett syndrome

NEW YORK, March 30, 2026 (GLOBE NEWSWIRE) -- Anavex Life Sciences Corp. (Anavex or the Company) (Nasdaq: AVXL), a... More