drugset / Trial / NCT02593773

Safety, Tolerability and Efficacy of ACTIMMUNE® Dose Escalation in Friedreich's Ataxia Study

NCT02593773

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this phase 3 multi-center, open-label extension study is to evaluate the long-term safety of ACTIMMUNE® (interferon-γ 1b) in participants with Friedreich's Ataxia.

Timeline

Start
2015-12-25
Primary completion
2017-03-21
Completion
2017-03-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Interferon gamma-1b Protein / enzyme biologic Subcutaneous

Indications