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Clinical trial

A Phase 2a, 2-part,Randomized, Double-blind, Placebo-controlled, Incomplete Block Crossover Study to Evaluate the Safety and Efficacy of VX-371 Solution for Inhalation With and Without Oral Ivacaftor in Subjects With Primary Ciliary Dyskinesia

NCT02871778 is registered in ClinicalTrials.gov with Parion Sciences as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 2a, 2-part,Randomized, Double-blind, Placebo-controlled, Incomplete Block Crossover Study to Evaluate the Safety and Efficacy of VX-371 Solution for Inhalation With and Without Oral Ivacaftor in Subjects With Primary Ciliary Dyskinesia
Lead sponsor
Parion Sciences
Phase
Phase 2
Overall status
Completed
Start date
August 31, 2016
Completion date
November 20, 2018
Enrollment
123 (actual)
Sites
34

Conditions

As the registry lists them; a condition with its own page is linked.

primary ciliary dyskinesia