Sarepta Therapeutics Announces Plan to Submit a New Drug Application (NDA) for Accelerated Approval of Golodirsen (SRP-4053) in Patients with Duchenne Muscular Dystrophy (DMD) Amenable to Skipping Exon 53

World News: . []

-- The Company met with the FDA Division of Neurology Products in February to obtain guidance on the regulatory pathway for golodirsen ---- The Company intends to complete a rolling NDA submission for golodirsen by year-end 2018 --CAMBRIDGE Mass March ...

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Globe Newswire: 11:30 GMT Monday 12th March 2018

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