Clinical Trial

Safety and Efficacy of KER-065 in Participants With Duchenne Muscular Dystrophy

Not Yet Recruiting Phase 2
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Summary
The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and efficacy of KER-065 administered to adult and pediatric ambulatory and nonambulatory male participants with Duchenne Muscular Dystrophy (DMD) on stable background therapy.
Trial Details
NCT Number NCT07704099
Lead Sponsor Keros Therapeutics, Inc.
Conditions Duchenne Muscular Dystrophy
Enrollment 36 participants
Start Date 2026-09-14
Primary Completion 2029-07-17 (estimated)
Study Completion 2029-08-14 (estimated)
Updated on ClinicalTrials.gov 2026-08-10