Join to learn about edasalonexent, a novel oral NF-kB inhibitor in development for the treatment of Duchenne muscular dystrophy, regardless of mutation type.
This webinar will include:
An update on the currently enrolling global Phase 3 PolarisDMD trial
An introduction to the open-label extension GalaxyDMD trial
You can advance the care, treatment and cure for Duchenne muscular dystrophy. Contributions in any amount can truly make a difference and can be credited to a fundraiser or event from the list below.
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