drugset / Trial / NCT03029455

A Study to Evaluate Safety and Pharmacokinetics of VX-659 in Healthy Subjects and in Adults With Cystic Fibrosis

NCT03029455 ↗

Phase 1 Completed 163 enrolled Vertex Pharmaceuticals Incorporated
RandomizedParallel-groupTriple-blindTreatment

Summary

Evaluate the safety and tolerability of VX-659 in healthy subjects

Timeline

Start
2016-11
Primary completion
2017-08
Completion
2017-08

Outcome

Met primary endpoint

paper VX-659-tezacaftor-ivacaftor resulted in significant mean increases in the percentage of predicted FEV1 through day 29 (P<0.001) PMID 30334693 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject BAMOCAFTOR Small molecule — Oral
Background Ivacaftor Other / unclassified — Oral
Background tezacaftor Other / unclassified — Oral

Indications