drugset / Trial / NCT01117012
Rollover Study of VX-770 in Cystic Fibrosis Subjects
Phase 3
Completed
192 enrolled
Vertex Pharmaceuticals Incorporated
Cystic Fibrosis Foundation · collab
NaSingle-groupOpen-labelTreatment
Summary
The primary objective of the study was to evaluate the safety of long-term VX-770 treatment in participants with cystic fibrosis (CF). The secondary objective of the study was to evaluate the efficacy of long-term VX-770 treatment in subjects with CF.
Timeline
- Start
- 2010-07
- Primary completion
- 2014-05
- Completion
- 2014-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ivacaftor | Other / unclassified | 150 mg | Oral |