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Clinical trial

A Phase 3, Open-label Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Lumacaftor in Combination With Ivacaftor in Subjects 6 Through 11 Years of Age With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation

NCT01897233 is registered in ClinicalTrials.gov with Vertex Pharmaceuticals Incorporated as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 3, Open-label Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Lumacaftor in Combination With Ivacaftor in Subjects 6 Through 11 Years of Age With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation
Lead sponsor
Vertex Pharmaceuticals Incorporated
Phase
Phase 3
Overall status
Completed
Start date
July 31, 2013
Completion date
October 31, 2015
Enrollment
62 (actual)
Sites
20

Conditions

As the registry lists them; a condition with its own page is linked.