by: Parent Project Muscular Dystrophy
PPMD and Catabasis as hosted a webinar on Wednesday, November 7 to discuss the Phase 3 PolarisDMD clinical trial studying edasalonexent in Duchenne muscular dystrophy, which is enrolling boys ages 4 to 7 (up to 8th birthday) regardless of mutation type who have not been on steroids for at least 6 months.
Topics included a discussion of the PolarisDMD clinical trial, endpoints, inclusion and exclusion criteria, and information on edasalonexent, including previous clinical results that showed preserved muscle function in boys affected by Duchenne with edasalonexent treatment compared to the off-treatment period as well as significantly improved biomarkers.
If you missed the live event, the recording can be found below.
