by: Parent Project Muscular Dystrophy
REGENXBIO joined PPMD for a community webinar on October 11, 2023 to discuss the company’s investigational gene therapy for Duchenne muscular dystrophy, AFFINITY DUCHENNE™, and AFFINITY BEYOND™, an AAV8 antibody assessment study. Jahannaz (Naz) Dastgir, DO, a pediatric neuromuscular specialist and the clinical development lead of the RGX-202 program at REGENXBIO, and Olivier Danos, PhD, Chief Scientific Officer at REGENXBIO, provided an overview of the recently announced interim data from the Phase I/II AFFINITY DUCHENNE™ trial of RGX-202, as well as answered questions from the community about these trials and future plans.
If you missed the live event, the recording can be viewed below:
