Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapies, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. The company is headquartered in Cambridge, Massachusetts. Show more
215 FIRST STREET, CAMBRIDGE, MA, UNITED STATES, 02142, Cambridge, MA, 02142, USA
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Market Cap
1.864B
52 Wk Range
$10.41 - $110.00
Previous Close
$17.40
Open
$17.56
Volume
1,554,996
Day Range
$17.50 - $18.19
Enterprise Value
2.263B
Cash
613.1M
Avg Qtr Burn
-14.59M
Insider Ownership
5.17%
Institutional Own.
88.40%
Qtr Updated
09/30/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
ELEVIDYS (SRP-9001) Details Duchenne muscular dystrophy | Approved Update | |
ELEVIDYS (delandistrogene moxeparvovec) Details Duchenne muscular dystrophy | Approved Update | |
EXONDYS 51 (eteplirsen) Details Duchenne muscular dystrophy | Approved Quarterly sales | |
AMONDYS 45 (casimersen) (SRP-4045) Details Duchenne muscular dystrophy | Approved Quarterly sales | |
VYONDYS 53 (golodirsen) Details Duchenne muscular dystrophy | Approved Quarterly sales | |
SRP-9003 Details Limb-Girdle Muscular Dystrophy (LGMD type 2E/R4) | Phase 3 Update | |
ELEVIDYS (delandistrogene moxeparvovec) Details Duchenne muscular dystrophy | Phase 3 Update | |
SRP-5051 (vesleteplirsen) Details Duchenne muscular dystrophy | Phase 2 Update | |
SRP-1001 Details Facioscapulohumeral muscular dystrophy (FSHD) | Phase 1/2 Data readout | |
SRP-1003 Details Myotonic dystrophy type 1 (DM1) | Phase 1/2 Data readout | |
SRP-1004 Details Spinocerebellar ataxia type 2 (SCA2) | Phase 1 Update | |
SRP-1005 Details Huntington’s Disease (HD) | Phase 1 Initiation | |
SRP-9005 Details Limb-Girdle Muscular Dystrophy (LGMD type 2C/R5) | Failed Discontinued | |
SRP-6004 Details Dysferlinopathy, Limb-Girdle Muscular Dystrophy | Failed Discontinued | |
SRP-9004 Details Limb-Girdle Muscular Dystrophy (LGMD type 2D/R3) | Failed Discontinued |
