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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics to Share Clinical Update for 30 mg/kg arm of MOMENTUM Study for SRP-5051, Its Investigational PPMO for the Treatment of Duchenne Muscular Dystrophy
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Sarepta Therapeutics to Announce First Quarter 2021 Financial Results and Recent Corporate Developments on May 5, 2021
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Sarepta Recommends Stockholders Reject the Below-Market Mini-Tender Offer by TRC Capital Investment Corporation
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Sarepta Therapeutics Announces Fourth Year of Route 79, The Duchenne Scholarship Program
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Sarepta Therapeutics (SRPT) Announces Limb-Girdle Muscular Dystrophy Treatement SRP-9003 Shows Sustained Expression and Functional Improvements 2 Years After Administration
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Sarepta Therapeutics’ Investigational Gene Therapy SRP-9003 for the Treatment of Limb-Girdle Muscular Dystrophy Type 2E Shows Sustained Expression and Functional Improvements 2 Years After Administr
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Sarepta Therapeutics to Present Results from its Gene Therapy and RNA Platforms at the 2021 Annual MDA Clinical and Scientific Conference
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Sarepta Therapeutics Announces Fourth Quarter and Full-Year 2020 Financial Results and Recent Corporate Developments
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics (SRPT) Announces FDA Approval of AMONDYS 45 (casimersen) Injection for the Treatment of Duchenne Muscular Dystrophyin Patients Amenable to Skipping Exon 45
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Sarepta Therapeutics Announces FDA Approval of AMONDYS 45™ (casimersen) Injection for the Treatment of Duchenne Muscular Dystrophy (DMD) in Patients Amenable to Skipping Exon 45
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Sarepta Therapeutics to Present at Upcoming Investor Conferences
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Sarepta Therapeutics to Announce Fourth Quarter and Full-Year 2020 Financial Results and Recent Corporate Developments on March 1, 2021
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Sarepta Therapeutics Announces Winners of the “Rare Lessons” Lesson Planning Competition
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics and Genevant Sciences Announce Research Collaboration for Lipid Nanoparticle-Based Gene Editing Therapeutics
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Sarepta Therapeutics to Present at the 39th Annual J.P. Morgan Healthcare Conference
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Sarepta Therapeutics (SRPT) Says Part 1 of Study SRP-9001-102 Met Primary Endpoint, But Did Not Achieve Statistical Significance in NSAA Total Score Improvement
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Sarepta Therapeutics Announces Top-line Results for Part 1 of Study 102 Evaluating SRP-9001, its Investigational Gene Therapy for the Treatment of Duchenne Muscular Dystrophy
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics Announces Executive Management Changes
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Sarepta Therapeutics (SRPT) Announces Positive Clinical Results from MOMENTUM, Phase 2 Clinical Trial of SRP-5051 in Patients with DMD Amenable to Skipping Exon 51
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Sarepta Therapeutics Announces Positive Clinical Results from MOMENTUM, a Phase 2 Clinical Trial of SRP-5051 in Patients with Duchenne Muscular Dystrophy Amenable to Skipping Exon 51
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Sarepta Therapeutics to Share Clinical Update for SRP-5051, its Investigational PPMO for the Treatment of Duchenne Muscular Dystrophy
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics to Present at the Evercore ISI 3rd Annual HealthCONx Virtual Conference
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Sarepta Therapeutics Named One of The Boston Globe’s Top Places to Work 2020
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Sarepta Therapeutics Announces Third Quarter 2020 Financial Results and Recent Corporate Developments
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Sarepta Therapeutics to Commence Dosing of the Next Study with Commercial Process Material for the SRP-9001 Gene Therapy Program for the Treatment of Duchenne Muscular Dystrophy
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Sarepta Therapeutics to Present at the 29th Annual Credit Suisse Virtual Healthcare Conference
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics to Announce Third Quarter 2020 Financial Results and Recent Corporate Developments on November 5, 2020
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Gene Therapy Company AavantiBio Launches with $107 Million Series A Financing from Perceptive Advisors, Bain Capital Life Sciences, RA Capital Management and Sarepta Therapeutics
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics (SRPT) Reports Sustained Functional Improvement Two Years After Treatment with SRP-9001, its Investigational Micro-dystrophin Gene Therapy for DMD
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Sarepta Therapeutics (SRPT) Investigational Gene Therapy SRP-9003 for LGMD2E Shows Sustained Functional Improvements 18-months After Administration
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Sarepta Therapeutics Investigational Gene Therapy SRP-9003 for the Treatment of Limb-Girdle Muscular Dystrophy Type 2E Shows Sustained Functional Improvements 18-months After Administration
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Sarepta Therapeutics Reports Sustained Functional Improvement Two Years After Treatment with SRP-9001, its Investigational Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy
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Sarepta Therapeutics Announces Recipients of Route 79, The Duchenne Scholarship Program
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Sarepta Therapeutics (SRPT) announces L-T functional data from its Most Advanced Gene Therapy Programs to be Presented at Upcoming Annual Congress of the World Muscle Society
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Long-term functional data from Sarepta Therapeutics’ Most Advanced Gene Therapy Programs to be Presented at Upcoming Annual Congress of the World Muscle Society
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Sarepta Therapeutics (SRPT) has completed Type C meeting with OTAT to obtain concurrence on commencement of its next clinical trial for SRP-9001
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Sarepta Therapeutics Provides Program Update for SRP-9001, its Investigational Gene Therapy for the Treatment of Duchenne Muscular Dystrophy
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Sarepta Therapeutics to Present at Upcoming Investor Conferences
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Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
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Sarepta Therapeutics (SRPT) Said FDA Accepted Casimersen (SRP-4045) NDA for Duchenne Muscular Dystrophy, Granted Priority Review Status
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Sarepta Therapeutics Announces FDA Acceptance of Casimersen (SRP-4045) New Drug Application for Patients with Duchenne Muscular Dystrophy Amenable to Skipping Exon 45
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Sarepta Therapeutics (SRPT), University of Florida Announce Collaboration to Accelerate the Discovery and Development of Therapies for Rare Genetic Diseases
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Sarepta Therapeutics and University of Florida Announce Collaboration to Accelerate the Discovery and Development of Therapies for Rare Genetic Diseases

