drugset / Trial / NCT02255552

Study of Eteplirsen in DMD Patients

NCT02255552 ↗

Phase 3 Completed 109 enrolled Sarepta Therapeutics, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The main objective of this study is to provide evidence of efficacy of eteplirsen (AVI-4658) in Duchenne muscular dystrophy (DMD) patients that are amenable to skipping exon 51. Additional objectives include evaluation of safety, biomarkers and the long-term effects of eteplirsen up to 96 weeks, followed by a safety extension (not to exceed 48 weeks).

Timeline

Start
2014-11-17
Primary completion
2019-06-14
Completion
2019-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Eteplirsen Antisense oligonucleotide 30 mg/kg Intravenous