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Phase 1/2Data readout

SRP-1001

Facioscapulohumeral muscular dystrophy (FSHD)

SRPTSarepta Therapeutics
Expected catalystDecember 31, 2026Company guidance: Dec 31, 2026

Catalyst overview

Event details

Drug or asset
SRP-1001
Development stage
Phase 1/2
Event type
Data readout
Indication
Facioscapulohumeral muscular dystrophy (FSHD)

Research summary

What is being tracked?

This catalyst tracks a Phase 1/2 data readout for SRP-1001 in Facioscapulohumeral muscular dystrophy (FSHD). The expected timing is based on the latest available company guidance and may change.

Development notes

8/6/25- Preliminary data in H2 2025. 11/03/25:- SAD enrollment complete, MAD cohort 6 ongoing; Ph1/2 SAD and MAD readouts for FSHD expected in early 2026. 02/25/26:- FSHD siRNA program highlighted among five clinical-stage RNA interference therapies with multiple readouts ahead. 03/25/26:- Early Ph1/2 ascending-dose results to be presented in webcast on March 25, 2026. 05/06/26:- First Ph1/2 SRP-1001 data in FSHD1 show dose-dependent exposure, early biomarker effects, and favorable tolerability. 08/05/26:- FSHD Phase 1/2 MAD cohort readouts remain expected in H2 2026.

Verification

Primary source

Confirm timing and program details against the company announcement or filing.

Open source

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SRP-1003

Myotonic dystrophy type 1 (DM1)

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Company

Sarepta Therapeutics

SRPT · NasdaqGS
Industry
Biotechnology
Pipeline assets
14
View SRPT research

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Updated Aug 23, 2026. Dates can change; this is not investment advice.

Disclaimer: Biotech Stock Intel is an independent research platform. Information is provided for informational purposes only and is not investment or medical advice. Always verify catalyst dates against primary sources and conduct your own research.
Biotech Stock Intel© 2026 Biotech Stock Intel
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