A one-year, Phase II, randomized, double-blind, placebo-controlled, safety and efficacy trial of edasalonexent in non-ambulatory boys and men affected by Duchenne Muscular Dystrophy
Latest Information Update: 26 Jul 2022
At a glance
- Drugs Edasalonexent (Primary)
- Indications Duchenne muscular dystrophy
- Focus Adverse reactions; Pharmacokinetics
Most Recent Events
- 10 Aug 2020 According to a Catabasis Pharmaceuticals media release, the the trial is expected to initiate in 2021.
- 10 Jan 2020 New trial record
- 08 Jan 2020 According to a Catabasis Pharmaceuticals media release, the company has entered into a collaboration with Duchenne UK to conduct this trial. Duchenne UK has granted over $600,000 in funding to support patient and clinical trial site costs for this trial. The company intends that upon completing this trial, patients will have the option to transition to the GalaxyDMD open-label extension trial and receive edasalonexent.