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SRPT

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  • Jefferies analysts described Sarepta Therapeutics as a potential turnaround story with catalysts extending into 2027 after updated Elevidys data showed clinically meaningful benefits in older ambulatory Duchenne muscular dystrophy patients.Oct 4, 2026

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News

  • Sarepta received FDA acceptance for sNDAs covering AMONDYS 45 and VYONDYS 53Jul 1, 2026
  • Sarepta announced it will present initial clinical data from its siRNA pipeline targeting FSHD1 and DM1Mar 25, 2026
  • Sarepta reported initial clinical data from its siRNA pipeline targeting FSHD1 and DM1Mar 25, 2026
  • Sarepta began screening and enrollment in ENDEAVOR Cohort 8 evaluating enhanced immunosuppression with ELEVIDYS gene therapy in non-ambulant Duchenne patientsMar 16, 2026
  • Sarepta Therapeutics received Clinical Trial Application approval for SRP-1005 Huntington's treatmentFeb 4, 2026

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