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Completed Phase 2 Interventional Results available

Clearing Lungs With ENaC Inhibition in Primary Ciliary Dyskinesia

ClinicalTrials.gov ID: NCT02871778

Public ClinicalTrials.gov record NCT02871778. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

To evaluate the safety and efficacy of treatment with VX-371 with and without ivacaftor, and the effect of VX-371 with and without ivacaftor on quality of life (QOL) in subjects with primary ciliary dyskinesia (PCD).

Study identification

NCT ID
NCT02871778
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Parion Sciences
Industry
Enrollment
123 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2016 (Actual)
Primary completion
Nov 20, 2018 (Actual)
Completion
Nov 20, 2018 (Actual)
Last update posted
Dec 16, 2021

2016 – 2018

United States locations

U.S. sites
21
U.S. states
19
U.S. cities
21
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Palo Alto California — —
Not listed Aurora Colorado — —
Not listed Washington D.C. District of Columbia — —
Not listed Miami Florida — —
Not listed Tampa Florida — —
Not listed Chicago Illinois — —
Not listed Indianapolis Indiana — —
Not listed Iowa City Iowa — —
Not listed Kansas City Kansas — —
Not listed Boston Massachusetts — —
Not listed Ann Arbor Michigan — —
Not listed Minneapolis Minnesota — —
Not listed Kansas City Missouri — —
Not listed St Louis Missouri — —
Not listed New York New York — —
Not listed Chapel Hill North Carolina — —
Not listed Cleveland Ohio — —
Not listed Philadelphia Pennsylvania — —
Not listed Columbia South Carolina — —
Not listed Seattle Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 13 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02871778, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 16, 2021 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02871778 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →