Sarepta Therapeutics (SRPT)

Overall impact
B (63)

Commentary

Sarepta Therapeutics is a strong overall performer. With a 'B' rating of 63.2 for overall impact (70th percentile compared to all companies), Sarepta Therapeutics ranks 368th out of 585 industry peers, behind Biogen, Ionis Pharmaceuticals, Gilead Sciences and 364 others, and ahead of Grifols, Jazz Pharmaceuticals, Bluebird Bio and 214 others. On top material causes for Sarepta Therapeutics's industry (Pharmaceuticals & Biotech), Sarepta Therapeutics performs well in Child and Maternal Health (93.3 score), Access to Affordable Healthcare (83.6), Child and Maternal Health (95.8) and 3 other causes where it received an 'A' score and performs poorly in Improved Mental Health (12.4 score), Humane Treatment of Animals (3.2), Decent, Safe Work Opportunities (25.6) and 1 other cause where it received a 'D' or 'F' score.
Impact
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Company
Founded
1980
Employees
835
Sector
Health Care
Industry
Biotechnology
Sub-industry
Biotechnology
SASB industry
Biotechnology & Pharmaceuticals
Headquarters
Ma, United States
Share classes
SRPT
Mission
To profoundly improve and extend the lives of patients with rare genetic-based diseases.
Description
Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 injection to treat Duchenne muscular dystrophy (Duchenne) in patients with confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; VYONDYS 53 for the treatment of Duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping; AMONDYS 45 for the treatment of Duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 45 skipping; and ELEVIDYS, an adeno-associated virus based gene therapy for the treatment of ambulatory pediatric patients with Duchenne with a confirmed mutation in the Duchenne gene. The company is also developing SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration and license agreements with F. Hoffman-La Roche Ltd; Arrowhead Pharmaceuticals, Inc.; University of Western Australia; Catalent Maryland, Inc.; Nationwide Children's Hospital; Dyno Therapeutics; Hansa Biopharma; Duke University; and Genethon. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.
Material causes
Ethos considers the following causes material for Sarepta Therapeutics, based on its industry sub-industry Biotechnology. Learn more about material causes in our methodology overview.

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