Catalyst: FDA OKs Duchenne Therapy Licensed from Santhera

 AGAMREE^® Indicated for the Treatment of Duchenne Muscular Dystrophy for Patients Aged Two Years and Older

Catalyst Holds the Exclusive North American License to Commercialize AGAMREE (vamorolone) for Duchenne Muscular Dystrophy and Other Potential Indications

Novel Corticosteroid With Favorable Side Effect Profile

Catalyst Expects to Commercially Launch AGAMREE in Q1 2024

AGAMREE Comprehensive Patient Assistance Program to Help Ensure Affordable Access for All DMD Patients Upon Commercial Launch

https://www.biospace.com/article/releases/catalyst-pharmaceuticals-reports-fda-approval-of-agamree-vamorolone-for-duchenne-muscular-dystrophy-granted-to-santhera-pharmaceuticals/