When the US Food and Drug Administration approved Mitsubishi Tanabe Pharma Corporation’s Radicava (edaravone) in 2017, it was the first treatment for amyotrophic lateral sclerosis to clear the agency in more than 20 years. The FDA is now considering Amylyx Pharmaceuticals, Inc.’s AMX0035 application for ALS, which is in some ways similar to that for edaravone. But the agency’s different views of the data show the difficulties in getting approval based on a single study.
The similarities in the studies for the two drugs was raised during the 30 March meeting of the FDA’s Peripheral...





