Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, siRNA platform, gene therapy, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients who have a confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an AAV-based gene therapy, which is contraindicated in patients with any deletion in exon 8 and/or exon 9 in the Duchenne gene. The company also develops SRP-9003, a gene therapy program for the treatment of LGMD2E; SRP-1001 to selectively target and knockdown DUX4 using RNAi in Phase 1/2a clinical trials; and SRP-1003 for reduction of expression of the DMPK gene in Phase 1/2a clinical trials. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Arrowhead Pharmaceuticals, Inc.; University of Western Australia; Nationwide Children's Hospital; Hansa Biopharma; and Duke University. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts. Show more
215 First Street, Cambridge, MA, 02142, United States
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Market Cap
1.754B
52 Wk Range
$10.42 - $103.32
Previous Close
$16.71
Open
$16.82
Volume
2,641,536
Day Range
$16.57 - $17.65
Enterprise Value
1.854B
Cash
939.7M
Avg Qtr Burn
N/A
Insider Ownership
5.16%
Institutional Own.
90.25%
Qtr Updated
12/31/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
ELEVIDYS (delandistrogene moxeparvovec) Details Duchenne muscular dystrophy | Approved Update | |
ELEVIDYS (SRP-9001) 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 | |
ELEVIDYS (delandistrogene moxeparvovec) Details Duchenne muscular dystrophy | Phase 3 Update | |
SRP-9003 Details Limb-Girdle Muscular Dystrophy (LGMD type 2E/R4) | Phase 3 Update | |
SRP-5051 (vesleteplirsen) Details Duchenne muscular dystrophy | Phase 2 Update | |
SRP-1003 Details Myotonic dystrophy type 1 (DM1) | Phase 1/2 Data readout | |
SRP-1001 Details Facioscapulohumeral muscular dystrophy (FSHD) | 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-6004 Details Dysferlinopathy, Limb-Girdle Muscular Dystrophy | Failed Discontinued | |
SRP-9004 Details Limb-Girdle Muscular Dystrophy (LGMD type 2D/R3) | Failed Discontinued | |
SRP-9005 Details Limb-Girdle Muscular Dystrophy (LGMD type 2C/R5) | Failed Discontinued |
