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Clinical Trial Summary

Assessment of the safety, tolerability and early signs of efficacy of three times a day orally administered BAY63-2521 in adult delta F508 homozygous Cystic Fibrosis patients not on treatment with Orkambi


Clinical Trial Description

The study consists of two parts. The first part is double-blind, randomized and placebo-controlled. The second part has an open-label study design. In part 1 patients on Orkambi or other CFTR-modulators are excluded. In part 2 patients on Orkambi are allowed to be included under certain conditions. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02170025
Study type Interventional
Source Bayer
Contact
Status Terminated
Phase Phase 2
Start date September 30, 2014
Completion date September 22, 2017

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