Nov 7 (Reuters) - Sarepta Therapeutics Inc:
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* Sarepta Therapeutics announces FDA clearance of IND for the company's ppmo exon 51 candidate, srp-5051
* Sarepta Therapeutics Inc - will immediately initiate its phase 1/2a clinical trial and begin screening patients with dmd amenable to skipping exon 51 Source text for Eikon: Further company coverage: