drugset / Trial / NCT00697073

Study to Assess the Safety and Tolerability of Idebenone in the Treatment of Friedreich's Ataxia Patients

NCT00697073

Phase 3 Completed 68 enrolled Santhera Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study is meant to assess the safety and tolerability of idebenone in patients with Friedreich's Ataxia over a 12 months period.

Timeline

Start
2008-07
Primary completion
2010-05
Completion
2010-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Idebenone Small molecule 1350 mg
Subject Idebenone Small molecule 2250 mg

Indications