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Completed Phase 3 Interventional Results available

A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD)

ClinicalTrials.gov ID: NCT01017952

Public ClinicalTrials.gov record NCT01017952. 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, 6:39 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

HZC102970: A 52-week Efficacy and Safety Study to Compare the Effect of Three Dosage Strengths of Fluticasone Furoate/GW642444 Inhalation Powder With GW642444 on the Annual Rate of Exacerbations 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 three strengths of the FF/GW642444 Inhalation Powder in subject with Chronic Obstructive Pulmonary Disease (COPD)

Study identification

NCT ID
NCT01017952
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,635 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
Sep 25, 2009 (Type not available)
Primary completion
Oct 1, 2011 (Actual)
Completion
Oct 17, 2011 (Actual)
Last update posted
Aug 31, 2018

2009 – 2011

United States locations

U.S. sites
89
U.S. states
30
U.S. cities
82
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35215 —
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Ozark Alabama 36360 —
GSK Investigational Site Tallassee Alabama 36078 —
GSK Investigational Site Chandler Arizona 85224 —
GSK Investigational Site Phoenix Arizona 85012 —
GSK Investigational Site Phoenix Arizona 85023 —
GSK Investigational Site Tucson Arizona 85723 —
GSK Investigational Site Fresno California 93710 —
GSK Investigational Site Fresno California 93726 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Monterey Park California 91754 —
GSK Investigational Site National City California 91950 —
GSK Investigational Site San Diego California 92117 —
GSK Investigational Site San Diego California 92128 —
GSK Investigational Site Torrance California 90502 —
GSK Investigational Site Torrance California 90505 —
GSK Investigational Site Van Nuys California 91405 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Thornton Colorado 80233 —
GSK Investigational Site Hartford Connecticut 06105 —
GSK Investigational Site Clearwater Florida 33765 —
GSK Investigational Site Cocoa Florida 32927 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Kissimmee Florida 34741 —
GSK Investigational Site Miami Florida 33183 —
GSK Investigational Site Pensacola Florida 32503 —
GSK Investigational Site St. Petersburg Florida 33707 —
GSK Investigational Site Tampa Florida 33603 —
GSK Investigational Site Winter Park Florida 32789 —
GSK Investigational Site Gainesville Georgia — —
GSK Investigational Site Martinez Georgia 30907 —
GSK Investigational Site Riverdale Georgia 30274 —
GSK Investigational Site Coeur d'Alene Idaho 83814 —
GSK Investigational Site Aurora Illinois 60504 —
GSK Investigational Site Elk Grove Village Illinois 60007 —
GSK Investigational Site Evansville Indiana 47713 —
GSK Investigational Site Evansville Indiana 47714 —
GSK Investigational Site Council Bluffs Iowa 51503 —
GSK Investigational Site Olathe Kansas 66061 —
GSK Investigational Site Topeka Kansas 66606 —
GSK Investigational Site Hazard Kentucky 41701 —
GSK Investigational Site Madisonville Kentucky 42431 —
GSK Investigational Site Brockton Massachusetts 02301 —
GSK Investigational Site Fall River Massachusetts 02720 —
GSK Investigational Site Pittsfield Massachusetts 01201 —
GSK Investigational Site Cadillac Michigan 49601 —
GSK Investigational Site Edina Minnesota 55438 —
GSK Investigational Site Fridley Minnesota 55432 —
GSK Investigational Site Columbia Missouri 65212 —
GSK Investigational Site Springfield Missouri 65803 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site St Louis Missouri 63143 —
GSK Investigational Site Lincoln Nebraska 68506 —
GSK Investigational Site Omaha Nebraska 68134 —
GSK Investigational Site Papillion Nebraska 68046 —
GSK Investigational Site Las Vegas Nevada 89106 —
GSK Investigational Site Cherry Hill New Jersey 08003 —
GSK Investigational Site Summit New Jersey 07091 —
GSK Investigational Site Albany New York 12205 —
GSK Investigational Site North Syracuse New York 13212 —
GSK Investigational Site Asheville North Carolina 28803 —
GSK Investigational Site Burlington North Carolina 27215 —
GSK Investigational Site Charlotte North Carolina 28207 —
GSK Investigational Site Statesville North Carolina 28625 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Centerville Ohio 45459 —
GSK Investigational Site Toledo Ohio 43614 —
GSK Investigational Site Portland Oregon 97220 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Charleston South Carolina 29406 —
GSK Investigational Site Columbia South Carolina 29201 —
GSK Investigational Site Easley South Carolina 29640 —
GSK Investigational Site Greenville South Carolina 29615 —
GSK Investigational Site Murrells Inlet South Carolina 29576 —
GSK Investigational Site Pelzer South Carolina 29669 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Nashville Tennessee 37232 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site New Braunfels Texas 78130 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Wichita Falls Texas 76309 —
GSK Investigational Site Newport News Virginia 23606 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Madison Wisconsin 53715 —

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 94 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01017952, 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 31, 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 NCT01017952 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →