Sarepta to present 3-year EMBARK trial data for Elevidys gene therapy in Duchenne muscular dystrophy at WMS 2026

By Public Technologies
  • Sarepta Therapeutics outlined new Duchenne muscular dystrophy data slated for presentation at the World Muscle Society congress Sept. 29-Oct. 3.
  • A late-breaking poster will cover efficacy and safety outcomes for its gene therapy in older ambulatory patients treated at ages 8-12.
  • Additional presentations will update longer-term outcomes from the EMBARK study, extending follow-up to three years post-infusion.
  • Separate posters will summarize pooled safety across Phase 1-3 trials, alongside Phase 3 results for golodirsen and casimersen versus placebo.


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