Tertiary Nav - Press Releases Press ReleasesMedia Statements Press Releases News Category Business & FinancialCitizenshipEarningsMedia StatementProduct NewsRecognitionRegulatoryScience & Innovation Year None202620252024202320222021202020192018201720162015201420132012201120102009200820072006 Date Title 3/31/26 Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) 3/25/26 Sarepta Announces First Clinical Data from siRNA Pipeline Targeting FSHD1 and DM1 3/24/26 Sarepta to Share First Clinical Data from siRNA Pipeline Targeting FSHD1 and DM1 3/19/26 Sarepta Provides Regulatory Update on AMONDYS 45® and VYONDYS 53® 3/16/26 Sarepta Announces that Screening and Enrollment are Underway in ENDEAVOR Cohort 8 to Evaluate Enhanced Immunosuppression Regimen as Part of ELEVIDYS Gene Therapy for Non-Ambulant Individuals with Duchenne 2/27/26 Sarepta Therapeutics Announces Call for Applications for the 9th Annual Route 79, The Duchenne Scholarship Program 2/26/26 Sarepta Therapeutics to Present New Long-Term and Safety Data Across Gene Therapy and Exon-Skipping Programs at 2026 Muscular Dystrophy Association Clinical & Scientific Congress 2/25/26 Sarepta Therapeutics Announces Fourth Quarter and Full-Year 2025 Financial Results and Recent Corporate Developments 2/24/26 Sarepta Therapeutics Announces Commercial Launch of ELEVIDYS in Japan 2/24/26 Sarepta Therapeutics to Present at the TD Cowen 46th Annual Health Care Conference 2/11/26 Sarepta Therapeutics to Announce Fourth Quarter and Full-Year 2025 Financial Results 2/4/26 Sarepta Therapeutics Announces Approval of Clinical Trial Application for SRP-1005, Its Investigational Treatment for Huntington’s Disease 1/26/26 Sarepta Announces Positive Topline Three-Year EMBARK Results Showing ELEVIDYS Significantly Slows Disease Progression on Key Functional Measures in Ambulatory Duchenne Patients 1/23/26 Sarepta Therapeutics to Report 3-Year Topline Data from EMBARK Study of ELEVIDYS Gene Therapy in Ambulatory Individuals with Duchenne Muscular Dystrophy 1/12/26 Sarepta Reports Preliminary* Fourth Quarter and Full-Year 2025 Net Product Revenues 1/7/26 Sarepta Therapeutics Announces Submission of Clinical Trial Application for SRP-1005, its Investigational Treatment for Huntington’s Disease 1/5/26 Sarepta Therapeutics to Present at the 44th Annual J.P. Morgan Healthcare Conference Toolkit Print Page | Email Alerts | RSS Feeds | Contacts
Press Releases News Category Business & FinancialCitizenshipEarningsMedia StatementProduct NewsRecognitionRegulatoryScience & Innovation Year None202620252024202320222021202020192018201720162015201420132012201120102009200820072006 Date Title 3/31/26 Sarepta Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) 3/25/26 Sarepta Announces First Clinical Data from siRNA Pipeline Targeting FSHD1 and DM1 3/24/26 Sarepta to Share First Clinical Data from siRNA Pipeline Targeting FSHD1 and DM1 3/19/26 Sarepta Provides Regulatory Update on AMONDYS 45® and VYONDYS 53® 3/16/26 Sarepta Announces that Screening and Enrollment are Underway in ENDEAVOR Cohort 8 to Evaluate Enhanced Immunosuppression Regimen as Part of ELEVIDYS Gene Therapy for Non-Ambulant Individuals with Duchenne 2/27/26 Sarepta Therapeutics Announces Call for Applications for the 9th Annual Route 79, The Duchenne Scholarship Program 2/26/26 Sarepta Therapeutics to Present New Long-Term and Safety Data Across Gene Therapy and Exon-Skipping Programs at 2026 Muscular Dystrophy Association Clinical & Scientific Congress 2/25/26 Sarepta Therapeutics Announces Fourth Quarter and Full-Year 2025 Financial Results and Recent Corporate Developments 2/24/26 Sarepta Therapeutics Announces Commercial Launch of ELEVIDYS in Japan 2/24/26 Sarepta Therapeutics to Present at the TD Cowen 46th Annual Health Care Conference 2/11/26 Sarepta Therapeutics to Announce Fourth Quarter and Full-Year 2025 Financial Results 2/4/26 Sarepta Therapeutics Announces Approval of Clinical Trial Application for SRP-1005, Its Investigational Treatment for Huntington’s Disease 1/26/26 Sarepta Announces Positive Topline Three-Year EMBARK Results Showing ELEVIDYS Significantly Slows Disease Progression on Key Functional Measures in Ambulatory Duchenne Patients 1/23/26 Sarepta Therapeutics to Report 3-Year Topline Data from EMBARK Study of ELEVIDYS Gene Therapy in Ambulatory Individuals with Duchenne Muscular Dystrophy 1/12/26 Sarepta Reports Preliminary* Fourth Quarter and Full-Year 2025 Net Product Revenues 1/7/26 Sarepta Therapeutics Announces Submission of Clinical Trial Application for SRP-1005, its Investigational Treatment for Huntington’s Disease 1/5/26 Sarepta Therapeutics to Present at the 44th Annual J.P. Morgan Healthcare Conference