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Completed Phase 3 Interventional Results available

Rollover Study of VX-770 in Cystic Fibrosis Subjects

ClinicalTrials.gov ID: NCT01117012

Public ClinicalTrials.gov record NCT01117012. 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 22, 2026, 6:26 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

An Open-Label, Rollover Study to Evaluate the Long Term Safety and Efficacy of VX-770 in Subjects With Cystic Fibrosis

Brief summary

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

The primary objective of the study was to evaluate the safety of long-term VX-770 treatment in participants with cystic fibrosis (CF). The secondary objective of the study was to evaluate the efficacy of long-term VX-770 treatment in subjects with CF.

Study identification

NCT ID
NCT01117012
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
192 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
6 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
Jun 30, 2010
Primary completion
Apr 30, 2014
Completion
Apr 30, 2014
Last update posted
Jul 6, 2015

2010 – 2014

United States locations

U.S. sites
36
U.S. states
24
U.S. cities
36
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Oakland California
Not listed Palo Alto California
Not listed San Diego California
Not listed Denver Colorado
Not listed Atlanta Georgia
Not listed Boise Idaho
Not listed Chicago Illinois
Not listed Indianapolis Indiana
Not listed Iowa City Iowa
Not listed Baltimore Maryland
Not listed Boston Massachusetts
Not listed Ann Arbor Michigan
Not listed Detroit Michigan
Not listed Minneapolis Minnesota
Not listed Kansas City Missouri
Not listed St Louis Missouri
Not listed Omaha Nebraska
Not listed Long Branch New Jersey
Not listed Buffalo New York
Not listed New Hyde Park New York
Not listed Syracuse New York
Not listed Cincinnati Ohio
Not listed Cleveland Ohio
Not listed Columbus Ohio
Not listed Toledo Ohio
Not listed Portland Oregon
Not listed Hershey Pennsylvania
Not listed Philadelphia Pennsylvania
Not listed Pittsburgh Pennsylvania
Not listed Knoxville Tennessee
Not listed Nashville Tennessee
Not listed Salt Lake City Utah
Not listed Chrlottesville Virginia
Not listed Seattle Washington
Not listed Morgantown West Virginia

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01117012, 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 6, 2015 · Synced Sep 22, 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 NCT01117012 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →