The FDA panel has voted down Sarepta Therapeutics Inc.’s (SRPT) Eteplirsen, proposed for the treatment of Duchenne muscular dystrophy amenable to exon 51 skipping.
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The FDA panel has voted down Sarepta Therapeutics Inc.’s (SRPT) Eteplirsen, proposed for the treatment of Duchenne muscular dystrophy amenable to exon 51 skipping.