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Wednesday, August 12, 2020

US FDA News: FDA Approves Targeted Treatment for Rare Duchenne Muscular Dystrophy Mutation

FDA has granted accelerated approval to Viltepso (viltolarsen) injection for the treatment of Duchenne muscular dystrophy in patients who have a confirmed mutation of the DMD gene that is amenable to exon 53 skipping.
Read more: FDA Approves Targeted Treatment for Rare Duchenne Muscular Dystrophy Mutation