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Sarepta Therapeutics Inc. (S1RP34 SA) stock market data APIs
Sarepta Therapeutics Inc. Financial Data Overview
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.
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Get Sarepta Therapeutics Inc. Fundamental Data
Sarepta Therapeutics Inc. Fundamental data includes:
- Net Revenue: 2 198 M
- EBITDA: -613 251 008
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- Latest Release: 2026-02-24
- EPS/Forecast: NaN
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Sarepta Therapeutics Inc. News
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How FDA Review of Sarepta’s ESSENCE Data At Sarepta Therapeutics (SRPT) Has Changed Its Investment Story
Sarepta Therapeutics recently updated investors that the FDA has agreed it can file supplemental applications by the end of April to seek conversion of AMONDYS 45 and VYONDYS 53 from accelerated to tr...
Sarepta Plans FDA Filings Seeking Full Approval for Two DMD Therapies
Sarepta Therapeutics SRPT announced plans to submit supplementary new drug applications (sNDAs) to the FDA for its two RNA-based PMO therapies — Amondys 45 and Vyondys 53 — by the end of next mont...
Sarepta Provides Regulatory Update on AMONDYS 45® and VYONDYS 53®
– Following feedback from FDA, Company intends to submit supplemental new drug applications to FDA by the end of April 2026 requesting conversion to traditional approval CAMBRIDGE, Mass., March 19,...
KROS Pipeline Catalysts: DMD Phase II and ALS Plans for 2026
Keros Therapeutics KROS enters 2026 with a clearer catalyst stack and a tighter operational focus. The near-term setup is led by rinvatercept, with study starts and regulatory interactions now mapped ...
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