Parent Project Muscular Dystrophy and Sarepta Therapeutics hosted a webinar on November 24, 2020 for a discussion about the SRP-9001 gene therapy development program. * This webinar recording contains edits to content requested by the company. Research & Clinical Trial Webinars,Webinars 4 years ago You may also like 43:52 MoveDMD: A Clinical Trial of Edasalonexent (CAT-1004) in Duchenne (June 2016) 9 years ago Research & Clinical Trial Webinars,Webinars 43:48 MissionDMD: FibroGen’s Anti-Fibrosis Program (May 2016) 9 years ago Research & Clinical Trial Webinars,Webinars 53:38 BMS Anti-Myostatin Adnectin Program (March 2016) 9 years ago Research & Clinical Trial Webinars,Webinars 1:13:48 HOPE-Duchenne Trial – Capricor Therapeutics (January 2016) 9 years ago Research & Clinical Trial Webinars,Webinars 1:00:42 Understanding the Potential of Epicatechin (December 2015) 9 years ago Research & Clinical Trial Webinars,Webinars 59:43 Understanding Myostatin Inhibition (November 2015) 9 years ago Research & Clinical Trial Webinars,Webinars 1:02:05 Decode Duchenne Genetic Testing Program (November 2015) 9 years ago Care Webinars,Webinars 1:01:24 PF-06252616 (Anti-Myostatin) Webinar (June 2015) 10 years ago Research & Clinical Trial Webinars,Webinars «1…2021222324…26»Page 22 of 26