SRPT - Sarepta Therapeutics

-

$undefined

N/A

(N/A)

Sarepta Therapeutics NASDAQ:SRPT Sarepta Therapeutics Inc. is leading a revolution in precision genetic medicine and every day is an opportunity to change the lives of people living with raredisease. The Company has built an impressive position in Duchenne muscular dystrophy (DMD) and in gene therapies for limb-girdle muscular dystrophies (LGMDs), mucopolysaccharidosis type IIIA, Charcot-Marie-Tooth (CMT), and other CNS-related disorders, with more than 40 programs in various stages of development. The Company's programs and research focus span several therapeutic modalities, including RNA, gene therapy and gene editing.

Location: 215 1st St Ste 415, Massachusetts, 02142-1213, US | Website: www.sareptatherapeutics.com | Industry: Pharmaceutical Preparation Manufacturing | Sector: Manufacturing


Market Cap

NaN

52 Wk Range

$ - $

Previous Close

$N/A

Open

$N/A

Day Range

N/A - N/A

Volume

N/A

Avg Volume

N/A

Enterprise Value

10.37B

Cash

1.198B

Avg Qtr Burn

-88.12M

Short % of Float

5.55%

Insider Ownership

4.81%

Institutional Own.

93.85%

Qtr Updated

09/30/24


Drug Pipeline

Powered by

Only showing assets and stage. See catalyst data with a free or premium account. Unlock more data with a free account.

Drug & IndicationStage & EventCatalyst Date
ELEVIDYS (SRP-9001) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

Approved

Quarterly sales

VYONDYS 53 (golodirsen) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

EXONDYS 51 (eteplirsen) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

ELEVIDYS (SRP-9001) Details
Duchenne muscular dystrophy

Approved

Quarterly sales

Phase 3

Data readout

ELEVIDYS (SRP-9001) Details
Duchenne muscular dystrophy

Phase 3

Update

SRP-5051 (vesleteplirsen) Details
Duchenne muscular dystrophy

Phase 2

Update

SRP-6004 Details
Dysferlinopathy, Limb-Girdle Muscular Dystrophy

Phase 1

Data readout