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Eteplirsen extension study in Duchenne muscular dystrophy

NCT03985878Phase 2Terminated

Sponsor
Sarepta Therapeutics
Start
Jun 2019
Primary completion
Aug 2022
Modality
Small Interfering RNA (siRNA), Modified DNA Oligonucleotides, Single-strand DNA
Countries
4
01

Overview

Phase 2, open-label, single-arm trial of eteplirsen in Duchenne muscular dystrophy (DMD), sponsored by Sarepta Therapeutics. Primary endpoints: Number of Participants Experiencing Adverse Events up to 162 weeks, Number of Participants Experiencing Death Due to Adverse Events up to 162 weeks and 1 more. Started Jun 2019; status: terminated.

02

Drugs

eteplirsen
03

Conditions

Duchenne muscular dystrophy (DMD)

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