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 50:36 Capricor Therapeutics’ HOPE-Duchenne Clinical Trial (November 2017) 7 years ago Research & Clinical Trial Webinars,Webinars 1:05:15 Wave Life Sciences (November 2017) 7 years ago Research & Clinical Trial Webinars,Webinars 59:29 FibroGen Update on Pamrevlumab & Enrolling Non-Ambulatory Study (October 2017) 7 years ago Research & Clinical Trial Webinars,Webinars 57:15 MoveDMD Trial Open-Label Extension Results (October 2017) 7 years ago Research & Clinical Trial Webinars,Webinars 1:01:20 Gene Therapy for Duchenne – PART 2: Nationwide Children’s Hospital (September 2017) 7 years ago Research & Clinical Trial Webinars,Webinars gene therapy 1:08:13 Gene Therapy for Duchenne (August 2017) 7 years ago Research & Clinical Trial Webinars,Webinars gene therapy 58:24 Nationwide Children’s Hospital Carrier Study (May 2017) 7 years ago Research & Clinical Trial Webinars,Webinars 59:04 Results from Phase I/II HOPE Clinical Trial of CAP-1002 (April 2017) 8 years ago Research & Clinical Trial Webinars,Webinars «1…1718192021…26»Page 19 of 26
by: Parent Project Muscular Dystrophy
