Overview

An Extension Study to Evaluate Casimersen or Golodirsen in Patients With Duchenne Muscular Dystrophy

Status:
Enrolling by invitation
Trial end date:
2026-08-10
Target enrollment:
0
Participant gender:
Male
Summary
The main objective of this study is to evaluate the safety and tolerability of long-term treatment with casimersen or golodirsen in patients with Duchenne muscular dystrophy (DMD).
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Sarepta Therapeutics
Sarepta Therapeutics, Inc.
Criteria
Inclusion Criteria:

- Completed a clinical trial evaluating casimersen or golodirsen, per protocol.

- Is between 7 and 23 years of age, inclusive, at enrollment.

Other inclusion/exclusion criteria apply.