drugset / Trial / NCT03532542

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

NCT03532542 ↗

Phase 3 Terminated 171 enrolled Sarepta Therapeutics, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

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).

Timeline

Start
2018-08-02
Primary completion
2023-07-26
Completion
2023-07-26

Outcome

Outcome not reported

Stopped: “The trial was stopped to reduce the clinical trial burden on participants while ensuring continued treatment via a post-trial access program with commercially available casimersen and golodirsen. Study was not terminated due to safety concerns.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Casimersen Unknown 30 mg/kg Intravenous
Subject Golodirsen Unknown 30 mg/kg Intravenous