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Completed Phase 2 Interventional Results available

A Study to Evaluate the Safety and Efficacy of VX-371 in Subjects With Cystic Fibrosis Who Are Homozygous for the F508del-CFTR Mutation

ClinicalTrials.gov ID: NCT02709109

Public ClinicalTrials.gov record NCT02709109. 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 Sep 2, 2026, 2:18 PM 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, Randomized, Double-blind, Placebo-controlled, Incomplete Block, Crossover Study to Evaluate the Safety and Efficacy of VX-371 in Subjects Aged 12 Years or Older With Cystic Fibrosis, Homozygous for the F508del-CFTR Mutation, and Being Treated With Orkambi

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of treatment with VX-371 in hypertonic saline compared to hypertonic saline alone in subjects with cystic fibrosis (CF) who are ≥12 years of age, homozygous for the F508del-cystic fibrosis transmembrane conductance regulator (CFTR) mutation, and being treated with Orkambi

Study identification

NCT ID
NCT02709109
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Parion Sciences
Industry
Enrollment
147 participants

Conditions and interventions

Interventions

Drug

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
Jan 31, 2016
Primary completion
Aug 31, 2017
Completion
Aug 31, 2017
Last update posted
Jul 28, 2021

2016 – 2017

United States locations

U.S. sites
30
U.S. states
19
U.S. cities
30
Facility City State ZIP Site status
Not listed Little Rock Arkansas
Not listed Oakland California
Not listed Gainesville Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Chicago Illinois
Not listed Glenview Illinois
Not listed Kansas City Kansas
Not listed New Orleans Louisiana
Not listed Worcester Massachusetts
Not listed Detroit Michigan
Not listed Grand Rapids Michigan
Not listed Minneapolis Minnesota
Not listed Jackson Mississippi
Not listed Lebanon New Hampshire
Not listed Albuquerque New Mexico
Not listed Albany New York
Not listed Hawthorne New York
Not listed Syracuse New York
Not listed Charlotte North Carolina
Not listed Cleveland Ohio
Not listed Pittsburgh Pennsylvania
Not listed Austin Texas
Not listed Dallas Texas
Not listed Fort Worth Texas
Not listed Tyler Texas
Not listed Charlottesville Virginia
Not listed Richmond Virginia
Not listed Madison Wisconsin
Not listed Milwaukee Wisconsin

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02709109, 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 Jul 28, 2021 · Synced Sep 2, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02709109 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →