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Clinical Trial Summary

This study will evaluate the safety and pharmacokinetics (PK) of lumacaftor (LUM) and ivacaftor (IVA) in participants 1 to less than 2 years of age with cystic fibrosis (CF), homozygous for F508del (F/F).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03601637
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact
Status Completed
Phase Phase 3
Start date September 7, 2018
Completion date October 29, 2021

See also
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