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Sarepta Announces FDA Acceptance of Golodirsen (SRP-4053) New Drug Application for Patients with Duchenne Muscular Dystrophy Amenable to Skipping Exon 53
Sarepta Therapeutics, Inc. (SRPT)
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Source: GlobeNewswire
Last sarepta therapeutics, inc. earnings: 2/26 04:05 pm
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US:NASDAQ Investor Relations: investorrelations.sarepta.com/events-and-presentations
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-- FDA Grants Priority Review Status -- -- Regulatory Action Date is August 19, 2019 -- -- Golodirsen has been studied for the treatment of exon 53 amenable patients,
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