drugset / Trial / NCT01381289

VX-770 Expanded Access Program

NCT01381289

Expanded access Approved for marketing Vertex Pharmaceuticals Incorporated

Summary

The purpose of this expanded access program is to provide VX-770 prior to its commercial availability to people with cystic fibrosis (CF) who have at least one copy of the G551D-CFTR mutation and who are in critical medical need and who are not eligible for participation in other Vertex-sponsored studies.

Timeline

Start
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Ivacaftor Other / unclassified 150 mg Oral

Indications