sarepta therapeutics

Leveraging Our United Voices: A Call To Collaborative Action Ahead of FDA’s Advisory Committee for SRP-9001

In September, Sarepta Therapeutics filed a BLA (Biologics License Application) for the approval of SRP-9001 (delandistrogene moxeparvovec), Sarepta’s investigational gene therapy for Duchenne muscular dystrophy, using the FDA’s accelerated approval pathway. During the marketing application’s…

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How You Can Be Involved in the First FDA Ad Comm Meeting for a Gene Therapy Product for Duchenne

Last week, Sarepta announced that the FDA Center for Biologics Evaluation and Research (CBER), Office of Therapeutic Products had informed the company that an advisory committee meeting will be scheduled prior to the PDUFA (or…

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Sarepta Therapeutics Announces Advisory Committee Meeting will be Held for SRP-9001

Sarepta Therapeutics today shared an update regarding SRP-9001 (delandistrogene moxeparvovec), Sarepta’s investigational gene therapy for Duchenne muscular dystrophy, for which a Biologics License Application (BLA) is currently under review by the U.S. Food and Drug…

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November 28, 2022

Sarepta Announces Biologics License Application (BLA) Accepted For Filing by the FDA for SRP-9001

PPMD is thrilled to learn that the FDA has accepted for filing and granted priority review for the Biologics License Application (BLA) for Sarepta’s gene therapy product, SRP-9001 (delandistrogene moxeparvovec) for the treatment of ambulant…

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September 29, 2022

Sarepta Therapeutics Submits Biologics License Application (BLA) for SRP-9001

Sarepta Therapeutics today announced it has submitted a Biologics License Application (BLA) to the FDA for the accelerated approval of SRP-9001 to treat ambulant patients with Duchenne. SRP-9001 is an investigational gene transfer therapy intended to deliver…

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September 14, 2022

WATCH: SRP-9001 Data Update from Studies 101, 102, and 103 (August 2022)

On August 24, 2022, PPMD was joined by Sarepta Therapeutics for a community webinar to present a SRP-9001 gene therapy data update from Studies 101, 102, and 103, following their recent presentation at a medical…

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September 13, 2022

Sarepta Shares EMBARK Study (SRP-9001-301) Enrollment Update

Sarepta Therapeutics, in partnership with Roche, has announced the EMBARK study of delandistrogene moxeparvovec (SRP-9001) in participants with Duchenne is now fully enrolled. Delandistrogene moxeparvovec (SRP-9001) is an investigational gene transfer therapy intended to deliver…

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September 6, 2022

Sarepta Therapeutics Announces That FDA has Lifted its Clinical Hold on SRP-5051

Sarepta Therapeutics has announced that the FDA has lifted the clinical hold on SRP-5051 (vesleteplirsen) following a serious adverse event of hypomagnesemia (low magnesium). SRP-5051 is Sarepta’s next-generation peptide-conjugated phosphorodiamidate morpholino oligomer (PPMO) to treat…

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Sarepta Announces Intent to Submit an Accelerated Approval Biologics License Application for SRP-9001

Sarepta Therapeutics today announced its intention to file for FDA approval of SRP-9001 this fall using the FDA’s accelerated approval pathway. SRP-9001 is an investigational gene transfer therapy intended to deliver the micro-dystrophin-encoding gene to muscle…

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Sarepta Shares New Functional Data From SRP-9001 Duchenne Gene Therapy Clinical Development Program

Sarepta Therapeutics has shared new functional data demonstrating functional improvements across multiple studies from the clinical development program for SRP-9001 including one-year functional results compared to an external control group, from Study SRP-9001-103 (ENDEAVOR) in…

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