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Completed Phase 2 Interventional Results available

A Study Evaluating the Safety and Efficacy of VX-440 Combination Therapy in Subjects With Cystic Fibrosis

ClinicalTrials.gov ID: NCT02951182

Public ClinicalTrials.gov record NCT02951182. 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 Jul 22, 2026, 12:00 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 2, Randomized, Double-blind, Controlled Study to Evaluate the Safety and Efficacy of VX-440 Combination Therapy in Subjects Aged 12 Years and Older With Cystic Fibrosis

Study identification

NCT ID
NCT02951182
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vertex Pharmaceuticals Incorporated
Industry
Enrollment
74 participants

Conditions and interventions

Interventions

  • TEZ Drug
  • IVA Drug
  • VX-440 Drug
  • Matched Placebo Drug

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
Sep 30, 2016
Primary completion
Jul 31, 2017
Completion
Jul 31, 2017
Last update posted
Aug 27, 2020

2016 – 2017

United States locations

U.S. sites
22
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
The Arizona Board of Regents on behalf of the University of Arizona Tucson Arizona
Stanford University Palo Alto California
University of California San Francisco California
National Jewish Health Denver Colorado
Joe Di Maggio Cystic Fibrosis & Pulmonary Center Hollywood Florida
Central Florida Pulmonary Group Orlando Florida
St. Luke's CF Center of Idaho Boise Idaho
Cystic Fibrosis Center of Chicago Glenview Illinois
The Johns Hopkins Hospital Baltimore Maryland
Boston Children's Hospital Boston Massachusetts
Massachusetts General Hospital Cystic Fibrosis Center Boston Massachusetts
University of Minnesota Minneapolis Minnesota
New York Medical College Hawthorne New York
Long Island Jewish Medical Center New Hyde Park New York
Columbia University Medical Center New York New York
Nationwide Children's Hospital Columbus Ohio
Respiratory Diseases of Children and Adolescents Oklahoma City Oklahoma
UPMC OSPARS Children's Hospital of Pittsburgh Pittsburgh Pennsylvania
Sanford Children's Specialty Clinic Sanford Research USD Sioux Falls South Dakota
The University of Texas Southwestern Center Dallas Texas
Children's Hospital of the Kings Daughters Norfolk Virginia
Seattle Children's Hospital 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 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02951182, 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 Aug 27, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02951182 live on ClinicalTrials.gov.

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