Vertex 809-011b

Trial Status: 
Closed

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

Purpose:

A study with Combination Therapy Ivacaftor and Lumacaftor in Children 6-11 for Cystic Fibrosis homozygote genotype DeltaF508. 

Sponsor:

Vertex Pharmaceuticals

Principal Investigator: 

Cori Daines, MD

Contact Information:

Osmara Y. Molina de Rodriguez, MS

Cell: (520) 891-6767 or Office: (520) 626-3910

Principal Investigator: 
Research Area: 
Clinical and Population Research