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

Biotechnology
Healthcare
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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 & IndicationStage & EventCatalyst Date

Approved

Update

ELEVIDYS (SRP-9001) Details
Duchenne muscular dystrophy

Approved

Update

EXONDYS 51 (eteplirsen) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

Approved

Quarterly sales

VYONDYS 53 (golodirsen) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

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