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On our #Q3Results call, CEO Doug Ingram discussed our third-quarter performance and shared an update on recent corporate developments.

On our #Q3Results call, Chief Customer Officer Dallan Murray shared details on an impressive third quarter, led by the continued strength of our gene therapy launch.

CEO Doug Ingram on Sarepta’s global licensing and collaboration agreement with Arrowhead Pharmaceuticals and how the agreement will help solidify Sarepta’s position as a genetic medicine leader.

Today we announced that enrollment & dosing is complete in Study SRP-9003-301, a Phase 3, multi-national, open-label study of investigational candidate SRP-9003 for the treatment of LGMD2E/R4. Data are expected in the first half of 2025.

Today at #JPM25, CEO Doug Ingram discussed our preliminary Q4 and full-year 2024 performance and shared an update on corporate developments.

Today, we released our financial results for Q4 and the full year of 2024, showing a 75% increase in net product revenue over the same quarter of the prior year. Our president and CEO on the results:

On this #RareDiseaseDay, we’re excited to announce the launch of Route 79, The Duchenne Scholarship Program. We’re awarding up to 20 scholarships to individuals living with Duchenne and up to 5 scholarships to siblings. Learn more: bit.ly/4khBJTs

Excited to be a partner of the 2025 Muscular Dystrophy Association Clinical & Scientific Conference. We’ll be there celebrating 75 years of #MDA impact & sharing updates on how Sarepta is advancing science for Duchenne and LGMD patients. #MDAconference

Excited to be here in Dallas at the 2025 Muscular Dystrophy Association Clinical & Scientific Conference sharing updates and connecting with the community. Come find us! #MDAconference #MDA #MuscularDystrophy

Today we issued a safety update for our approved gene therapy. Read here: bit.ly/4iqEekG

Today we shared updates from our clinical programs focused on limb-girdle muscular dystrophy (LGMD) subtypes 2C/R5, 2D/R3 and 2E/R4. Read more here: bit.ly/3G9VEUV

Are you in New Orleans for #ASGCT2025? Come find us at booth 1513, explore our posters and oral presentations and learn about our commitment to advancing precision genetic medicine for rare disease. Learn more here: annualmeeting.asgct.org

Attending #ASGCT2025? Explore our posters and oral presentations. Learn more here: annualmeeting.asgct.org

News: The U.S. FDA granted Platform Technology Designation to SRP-9003, Sarepta’s investigational gene therapy for the treatment of LGMD type 2E/R4. This is one of the first programs to receive the technology designation. Read more at Sarepta.com.

Read the statement at Sarepta.com.