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Completed Phase 3 Interventional Results available

Efficacy and Safety Study of Fluticasone Furoate (FF)/GW642444 Inhalation Powder and the Individual Components in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT01054885

Public ClinicalTrials.gov record NCT01054885. 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 30, 2026, 5:57 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 24-Week Study to Evaluate the Efficacy and Safety of Fluticasone Furoate (FF)/GW642444 Inhalation Powder and the Individual Components Delivered Once Daily (AM) Via a Novel Dry Powder Inhaler Compared With Placebo in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

Brief summary

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

The Purpose of this study is to assess the efficacy and safety of two strengths of the FF/GW642444 Inhalation Powder in subject with Chronic Obstructive Pulmonary Disease (COPD)

Study identification

NCT ID
NCT01054885
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,226 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 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 19, 2009 (Type not available)
Primary completion
Feb 1, 2011 (Actual)
Completion
Feb 8, 2011 (Actual)
Last update posted
Jan 24, 2018

2009 – 2011

United States locations

U.S. sites
49
U.S. states
19
U.S. cities
49
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35235 —
GSK Investigational Site Jasper Alabama 35501 —
GSK Investigational Site Lakewood California 90712 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Monterey Park California 91754 —
GSK Investigational Site National City California 91950 —
GSK Investigational Site Oxnard California 93030-5841 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site Santa Monica California 90404 —
GSK Investigational Site Wilmington Delaware 19805 —
GSK Investigational Site Bay Pines Florida 33744 —
GSK Investigational Site Brandon Florida 33511 —
GSK Investigational Site Clearwater Florida 33756 —
GSK Investigational Site Cocoa Florida 32927 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Pensacola Florida 32503 —
GSK Investigational Site Decatur Georgia — —
GSK Investigational Site Gainesville Georgia — —
GSK Investigational Site Martinez Georgia 30907 —
GSK Investigational Site Lenexa Kansas 66215 —
GSK Investigational Site Wheaton Maryland 20902 —
GSK Investigational Site Saint Charles Missouri 63301 —
GSK Investigational Site Cherry Hill New Jersey 08003 —
GSK Investigational Site Ocean City New Jersey 7712 —
GSK Investigational Site Brooklyn New York 11229 —
GSK Investigational Site Elizabeth City North Carolina 27909 —
GSK Investigational Site Statesville North Carolina 28625 —
GSK Investigational Site Cincinnati Ohio 45231 —
GSK Investigational Site Dayton Ohio 45439 —
GSK Investigational Site Oklahoma City Oklahoma 73103 —
GSK Investigational Site Tulsa Oklahoma 74136-8303 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Portland Oregon 97213 —
GSK Investigational Site Columbia South Carolina 29203 —
GSK Investigational Site Easley South Carolina 29640 —
GSK Investigational Site Gaffney South Carolina 29340 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Seneca South Carolina 29678 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Union South Carolina 29379 —
GSK Investigational Site Johnson City Tennessee 37601 —
GSK Investigational Site New Tazewell Tennessee 37825 —
GSK Investigational Site Boerne Texas 78006 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Kingwood Texas 77339 —
GSK Investigational Site Temple Texas 76508 —
GSK Investigational Site Fredericksburg Virginia 22401 —
GSK Investigational Site Morgantown West Virginia 26505 —

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 100 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01054885, 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 Jan 24, 2018 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01054885 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →