drugset / Trial / NCT01117012

Rollover Study of VX-770 in Cystic Fibrosis Subjects

NCT01117012

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

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 150 mg Oral

Indications