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 1:04:43 The Heart of the Matter – PPMD’s Research Priorities (December 2018) 6 years ago Research & Clinical Trial Webinars,Webinars 1:01:12 Engaging Families in Care Guideline Development (November 2018) 6 years ago Care Webinars,Research & Clinical Trial Webinars,Webinars 47:47 PolarisDMD: Phase 3 Clinical Trial of Edasalonexent, a Novel NF-kB Inhibitor (November 2018) 6 years ago Research & Clinical Trial Webinars,Webinars 1:45 Gene Therapy & Duchenne Muscular Dystrophy 6 years ago General Information gene therapy 56:15 An Update on Corticosteroids (October 2018) 6 years ago Care Webinars,Research & Clinical Trial Webinars,Webinars 44:29 Is Myostatin Still a Potential Therapeutic Target? (October 2018) 6 years ago Research & Clinical Trial Webinars,Webinars 1:00:51 Puberty and Duchenne (September 2018) 6 years ago Care Webinars,Webinars 1:09:04 HOPE-2 Duchenne Clinical Trial – Capricor (July 2018) 6 years ago Research & Clinical Trial Webinars,Webinars «1…1516171819…26»Page 17 of 26
by: Parent Project Muscular Dystrophy
