Company profile

SAREPTA THERAPEUTICS, INC.

NASDAQ:SRPTBiotechnology: Pharmaceutical Preparations

Drug pipeline (9)

AssetStageRevenueTrialsStatus
ELEVIDYSapproved$98.1MQ2 20260—
AMONDYS 45approved—1approved
EXONDYS 51approved—8approved
VYONDYS 53approved—3approved
BIDRIDISTROGENE XEBOPARVOVECphase3—3active

Revenue is the latest quarter the company reported for that product, from SEC filings; a fourth quarter is the year less nine months when no filing states one. Trial counts are of the product's ingredients, deduplicated by trial, so products sharing an ingredient share trials.

Clinical trials (49)

NCT IDPhaseStatusStartCompletionSponsor nameTitle
NCT07536061phase1recruiting2026-05-122027-11-30Sarepta Therapeutics, Inc.A First-in-human Study of the Effects of SRP-1005 in Participants With Huntington's Disease
NCT05876780phase1active_not_recruiting2022-12-192028-08-28Sarepta Therapeutics, Inc.A Gene Transfer Single Dose Study to Evaluate the Safety, Tolerability and Efficacy of SRP-9003 in Non-Ambulatory and Ambulatory Participants With Limb Girdle Muscular Dystrophy, Type 2E/R4 (Beta-Sarcoglycan [β-SG] Deficiency)
NCT05906251phase1terminated2023-05-222025-06-13Sarepta Therapeutics, Inc.A Gene Transfer Study to Evaluate the Safety, Tolerability and Efficacy of SRP-6004 in Ambulatory Participants With Limb Girdle Muscular Dystrophy, Type 2B/R2 (LGMD2B/R2, Dysferlin [DYSF] Related)
NCT06241950phase1terminated2024-01-292025-10-10Sarepta Therapeutics, Inc.A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) Following Imlifidase Infusion in Participants With Duchenne Muscular Dystrophy (DMD) Determined to Have Pre-existing Antibodies to Recombinant Adeno-Associated Virus Serotype (rAAVrh74)
NCT05881408phase3active_not_recruiting2023-05-312027-05-31Sarepta Therapeutics, Inc.A Gene Transfer Therapy Study to Evaluate the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Non-Ambulatory and Ambulatory Participants With Duchenne Muscular Dystrophy (DMD)

FDA applications (4)

ApplicationApprovedTypeApplicantProducts
BLA 1257812023-06-22BLASAREPTA THERAPEUTICS, INC.
NDA 2130262021-02-25NDASAREPTA THERAPEUTICS INC
NDA 2119702019-12-12NDASAREPTA THERAPEUTICS INC
NDA 2064882016-09-19NDASAREPTA THERAPEUTICS INC