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Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of LUM/IVA combination therapy in subjects 12 years and older with CF and advanced lung disease and who are homozygous for the F508del CFTR mutation


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02390219
Study type Interventional
Source Vertex Pharmaceuticals Incorporated
Contact
Status Completed
Phase Phase 3
Start date March 2015
Completion date October 2016

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