A second advisory committee meeting to consider additional information about Amylyx Pharmaceuticals, Inc.’s amyotrophic lateral sclerosis (ALS) drug AMX0035 may be an attempt by the US Food and Drug Administration to keep the public updated about new application information, and could be a sign that the agency is adapting its approach in the wake of criticism of how it handled the approval of Aduhelm.
Amylyx announced on 5 July that another Peripheral and Central Nervous System Drugs Advisory Committee meeting would be held on...





