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Completed Phase 3 Interventional Results available

Fluticasone Furoate/GW642444 Inhalation Powder Long-Term Safety Study

ClinicalTrials.gov ID: NCT01018186

Public ClinicalTrials.gov record NCT01018186. 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, 4:25 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 Randomized, Double-Blind, Double Dummy, Active Comparator, Parallel Group, Multicenter Study to Evaluate the Safety of Once-Daily Fluticasone Furoate/GW642444 Inhalation Powder for 52 Weeks in Adolescent and Adult Subjects With Asthma

Brief summary

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

The purpose of this study is to evaluate the long-term safety of fluticasone furoate/GW642444

Study identification

NCT ID
NCT01018186
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
503 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
Oct 18, 2009
Primary completion
Apr 30, 2011
Completion
May 11, 2011
Last update posted
Feb 14, 2018

2009 – 2011

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
GSK Investigational Site Oxford Alabama 36203
GSK Investigational Site Huntington Beach California 92647
GSK Investigational Site Mission Viejo California 92691
GSK Investigational Site Rolling Hills Estates California 90274
GSK Investigational Site Stockton California 95207
GSK Investigational Site Bethesda Maryland 20814
GSK Investigational Site Bellevue Nebraska 68123-4303
GSK Investigational Site Skillman New Jersey 08558
GSK Investigational Site Raleigh North Carolina 27607
GSK Investigational Site Cincinnati Ohio 45231
GSK Investigational Site Oklahoma City Oklahoma 73103
GSK Investigational Site Austin Texas 78750
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site El Paso Texas 79903
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Waco Texas 76712
GSK Investigational Site South Burlington Vermont 05403
GSK Investigational Site Greenfield Wisconsin 53228

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 29 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01018186, 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 Feb 14, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01018186 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →