drugset / Trial / NCT03603288

Phase III Study With Idebenone in Patients With Duchenne Muscular Dystrophy (SIDEROS-E)

NCT03603288 ↗

Phase 3 Terminated 161 enrolled Santhera Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to assess the long-term safety and efficacy of idebenone in patients with Duchenne muscular dystrophy (DMD) who completed the SIDEROS study.

Timeline

Start
2018-07-04
Primary completion
2020-11-25
Completion
2020-11-25

Outcome

Outcome not reported

Stopped: “Interim analysis concluded to futility of main study SIDEROS (SNT-III-012)”

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Idebenone Small molecule 900 mg —