News Releases

Date Title and Summary Additional Formats
Toggle Summary Sarepta Therapeutics and Nationwide Children’s Hospital Announce FDA Clearance of IND for Micro-Dystrophin Gene Therapy Program for the Treatment of Duchenne Muscular Dystrophy
-- Nationwide Children’s Hospital to initiate a Phase 1/2a clinical trial at potentially therapeutic doses in children with DMD by mid-November 2017 -- -- First micro-dystrophin gene therapy program in clinical development for DMD -- CAMBRIDGE, Mass. , Nov.
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Toggle Summary Sarepta Therapeutics and Nationwide Children’s Hospital Announce U.S. Food and Drug Administration (FDA) Clearance of the IND Application for the GALGT2 Gene Therapy Program
-- Nationwide Children’s Hospital is on track to initiate a Phase 1/2a clinical trial in individuals with Duchenne muscular dystrophy (DMD) by year-end 2017 -- CAMBRIDGE, Mass. , Nov. 03, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company
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Toggle Summary Sarepta Therapeutics to Present at the 26th Annual Credit Suisse Healthcare Conference
CAMBRIDGE, Mass. , Nov. 01, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases, today announced that management will present at
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Toggle Summary Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
CAMBRIDGE, Mass. , Oct. 31, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases, granted equity awards on October 31, 2017 , that
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Toggle Summary Sarepta Therapeutics Signs Exclusive Global Collaboration with Duke University for Gene Editing CRISPR/Cas9 Technology to Develop New Treatments for Duchenne Muscular Dystrophy (DMD)
-- Exclusive license option grants Sarepta rights to Duke intellectual property for CRISPR/Cas9 -- CAMBRIDGE, Mass. , Oct. 31, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision
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Toggle Summary Sarepta Therapeutics Announces Third Quarter 2017 Financial Results and Recent Corporate Developments
-- Third quarter 2017 EXONDYS 51® (eteplirsen) total net revenues of $46 million -- -- Company raises annual 2017 revenue guidance to between $150 million and $155 million -- CAMBRIDGE, Mass. , Oct. 25, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc.
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Toggle Summary Sarepta Therapeutics to Announce Third Quarter 2017 Financial Results and Recent Corporate Developments on October 25, 2017
CAMBRIDGE, Mass. , Oct. 16, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases, will report third quarter 2017 financial results
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Toggle Summary Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
CAMBRIDGE, Mass. , Sept. 29, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases, granted equity awards on September 25, 2017 ,
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Toggle Summary Sarepta Therapeutics to Present at the 22nd International Annual Congress of the World Muscle Society
CAMBRIDGE, Mass. , Sept. 28, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc. (NASDAQ:SRPT), a commercial-stage biopharmaceutical company focused on the discovery and development of precision genetic medicines to treat rare neuromuscular diseases, will present a total of six posters at the 22 nd
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Toggle Summary Sarepta Therapeutics Appoints Guriqbal S. Basi, Ph.D. as Chief Scientific Officer
The appointment of Dr. Basi, formerly the chief science and technology officer of Elan, continues to strengthen Sarepta’s leadership team as it accelerates the advancement of its rare disease pipeline CAMBRIDGE, Mass. , Sept. 25, 2017 (GLOBE NEWSWIRE) -- Sarepta Therapeutics, Inc.
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