May 2, 2018 / Clinical Trials

May 9 Webinar: Introducing PPMO – The Future of Precision RNA-Targeted Therapies for Duchenne

Sarepta Therapeutics, Inc. will join Parent Project Muscular Dystrophy for a webinar update on Wednesday, May 9 at 1:00 PM EDT to discuss PPMO, Sarepta’s next generation precision RNA-targeting therapeutic platform for use in Duchenne muscular dystrophy.

Sarepta will also introduce their planned innovative enhancements to the trial design for their actively enrolling Phase 1 clinical trial, 5051-101, for their PPMO exon 51 candidate (SRP-5051, NCT: 03375255), and outline their plans for future development of additional exon targets.


  • Pat Furlong
    Founding President & CEO, Parent Project Muscular Dystrophy


  • Doug Ingram
    President and CEO, Sarepta Therapeutics, Inc.
    Please submit questions in advance to (subject line: Sarepta Webinar) by Monday, May 7 at 12pm eastern.

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