SRPT
Sarepta Therapeutics, Inc. · Healthcare
Insiders sold $417K of Sarepta Therapeutics, Inc. in the last 12 months and bought none
SRPT over the last year
SRPT after insider buys
3 months after each buy, from the first price a copier could get.
7 buys since 2017 with 3 months of prices.
Congress
Members reported 3 trades in SRPT since 2023.
Every filing
74 insider filings since 2016, newest first
Douglas S Ingram · President and CEO
Sandesh Mahatme · EVP, CFO, CBO
Douglas S Ingram · President and CEO
David T Howton · SVP and General Counsel
Alexander Cumbo · SVP and Chief Commercial Officer
Richard Barry · Director
Hans Lennart Rudolf Wigzell · Director
Douglas S Ingram · President and CEO
Shamim Ruff · SVP, Regulatory Affairs, Qual
Shamim Ruff · SVP, Regulatory Affairs, Qual
Douglas S Ingram · President and CEO
Edward M. Md Kaye · Director
David T Howton · SVP and General Counsel
Alexander Cumbo · SVP and Chief Commercial Officer
Sandesh Mahatme · EVP, CFO, CBO
Shamim Ruff · SVP, Regulatory Affairs, Qual
Sandesh Mahatme · SVP and CFO
Shamim Ruff · SVP, Regulatory Affairs, Qual
Edward M. Md Kaye · President, CEO and CMO
David T Howton · SVP and General Counsel
Edward M. Md Kaye · President, CEO and CMO
David T Howton · SVP and General Counsel
Jayant Aphale · VP, Technical Operations
Edward M. Md Kaye · SVP Interim CEO, CMO
About Sarepta Therapeutics, Inc.
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.
Filings come from SEC EDGAR and prices from daily closes. Not investment advice.