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Completed Phase 3 Interventional Results available

Asthma Exacerbation Study

ClinicalTrials.gov ID: NCT01086384

Public ClinicalTrials.gov record NCT01086384. 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 18, 2026, 3:19 AM 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 Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects With Asthma

Brief summary

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

This study will establish the safety as well as demonstrate benefit of the addition of a LABA to an ICS by utilizing an endpoint (time to first severe asthma exacerbation) that informs on both safety and efficacy.

Study identification

NCT ID
NCT01086384
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
2,020 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
Feb 22, 2010 (Type not available)
Primary completion
Sep 1, 2011 (Actual)
Completion
Sep 15, 2011 (Actual)
Last update posted
Jan 24, 2018

2010 – 2011

United States locations

U.S. sites
64
U.S. states
23
U.S. cities
61
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Oxford Alabama 36203 —
GSK Investigational Site Phoenix Arizona 85016 —
GSK Investigational Site Scottsdale Arizona 85251 —
GSK Investigational Site Tucson Arizona 85724-5073 —
GSK Investigational Site Bell Gardens California 90201 —
GSK Investigational Site Fresno California 93721 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Mission Viejo California 92691 —
GSK Investigational Site Napa California 94558 —
GSK Investigational Site Rancho Mirage California 92270 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site Roseville California 95661 —
GSK Investigational Site San Diego California 92120 —
GSK Investigational Site Stockton California 95207 —
GSK Investigational Site Torrance California 90505 —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Englewood Colorado 80112 —
GSK Investigational Site Cocoa Florida 32927 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Valrico Florida 33596 —
GSK Investigational Site Winter Park Florida 32789 —
GSK Investigational Site Albany Georgia 31707 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Lawrenceville Georgia 30046 —
GSK Investigational Site Coeur d'Alene Idaho 83814 —
GSK Investigational Site River Forest Illinois 60305 —
GSK Investigational Site Indianapolis Indiana 46256 —
GSK Investigational Site Hazard Kentucky 41701 —
GSK Investigational Site Owensboro Kentucky 42301 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Baltimore Maryland 21236 —
GSK Investigational Site Rockville Centre New York 11570 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Canton Ohio 44718 —
GSK Investigational Site Cincinnati Ohio 45231 —
GSK Investigational Site Sylvania Ohio 43560 —
GSK Investigational Site Oklahoma City Oklahoma 73103 —
GSK Investigational Site Oklahoma City Oklahoma 73120 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Collegeville Pennsylvania 19426 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site Philadelphia Pennsylvania 19115 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Charleston South Carolina 29407 —
GSK Investigational Site Gaffney South Carolina 29340 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Union South Carolina 29379 —
GSK Investigational Site Knoxville Tennessee 37909 —
GSK Investigational Site Austin Texas 78750 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site Houston Texas 77074 —
GSK Investigational Site Killeen Texas 76542 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Waco Texas 76712 —
GSK Investigational Site South Burlington Vermont 05403 —
GSK Investigational Site Bellingham Washington 98225 —
GSK Investigational Site La Crosse Wisconsin 54601 —

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 119 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01086384, 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 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01086384 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →