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BRIEF-Sarepta Therapeutics reports FDA clearance of IND for co's ppmo exon 51 candidate, srp-5051

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:

Read the original article on Reuters. Copyright 2017. Follow Reuters on Twitter.
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