A Phase 2, Randomized, Double-blind Study to Evaluate the Efficacy and Safety of VX-561 in Subjects Aged 18 Years and Older With Cystic Fibrosis
Principal Investigator
Study Number
F19067
Summary
The purpose of this study is to evaluate the efficacy, safety, pharmacodynamic (PD) and pharmacokinetic (PK) effect of VX-561.
Phase
N/A
Contact
Available at the following location(s)
- Manchester
View more details at ClinicalTrials.gov
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