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In Wake of Prosensa Failure

Oh, Skip It? FDA View Changing; Sarepta’s DMD Efforts Hit Hard

By Randy Osborne
Staff Writer

Tuesday, November 12, 2013
The FDA altered its view of Sarepta Therapeutics Inc.’s data with exon-skipping therapy eteplirsen for Duchenne muscular dystrophy (DMD) after Prosensa Holding NV’s failure with exon-skipper drisapersen for the condition, but Sarepta CEO Chris Garabedian hopes the agency can still be brought around.

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