Trial intelligence / Profile preview

Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy

2018-000464-29Phase 3Completed

Sponsor
Astria Therapeutics
Start
Sep 2018
Modality
Peptide-Drug Conjugates → Peptide Conjugates → Peptides, Small Molecules
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in Duchenne muscular dystrophy (DMD) comparing Edasalonexent with Placebo (2 arms). Primary endpoint: Change from baseline in North Star Ambulatory Assessment. Started Sep 2018; status: completed.

02

Drugs

edasalonexent
03

Conditions

Duchenne muscular dystrophy (DMD)

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