drugset / Trial / NCT02593773
Safety, Tolerability and Efficacy of ACTIMMUNE® Dose Escalation in Friedreich's Ataxia Study
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Interferon gamma-1b | Protein / enzyme biologic | — | Subcutaneous |