drugset / Trial / NCT03218995

Study of Eteplirsen in Young Participants With Duchenne Muscular Dystrophy (DMD) Amenable to Exon 51 Skipping

NCT03218995 ↗

Phase 2 Completed 15 enrolled Sarepta Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, dose-escalation study to evaluate the safety, tolerability, and PK of once-weekly IV infusions of eteplirsen in approximately 12 male participants, ages 6 months to 48 months (inclusive), who have genotypically confirmed DMD with a deletion mutation amenable to exon 51 skipping.

Timeline

Start
2017-08-16
Primary completion
2021-03-10
Completion
2021-03-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Eteplirsen Antisense oligonucleotide 30 mg/kg Intravenous