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Completed Phase 3 Interventional Results available

HZA113091 Efficacy and Safety of Fluticasone Furoate/Vilanterol (GW642444) in Adults and Adolescents

ClinicalTrials.gov ID: NCT01147848

Public ClinicalTrials.gov record NCT01147848. 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 19, 2026, 2:01 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 Randomised, Double-blind, Double-dummy, Parallel-group Multicentre Study to Assess Efficacy and Safety of Fluticasone Furoate/GW642444 Inhalation Powder and Fluticasone Propionate/Salmeterol Inhalation Powder in the Treatment of Persistent Asthma in Adults and Adolescents

Brief summary

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

The purpose of the study is to compare the efficacy and safety of fluticasone furoate/vilanterol (GW642444) inhalation powder administered once daily with fluticasone propionate/salmeterol administered twice daily in adolescent and adult subjects 12 years of age and older with persistent bronchial asthma over a 24-week period.

Study identification

NCT ID
NCT01147848
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
810 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
Jun 2010 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Jul 2011 (Actual)
Last update posted
Jan 18, 2017

2010 – 2011

United States locations

U.S. sites
25
U.S. states
12
U.S. cities
24
Facility City State ZIP Site status
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site San Diego California 92117 —
GSK Investigational Site Centennial Colorado 80112 —
GSK Investigational Site Denver Colorado 80230 —
GSK Investigational Site Cocoa Florida 32927 —
GSK Investigational Site Bethesda Maryland 20814 —
GSK Investigational Site Wheaton Maryland 20902 —
GSK Investigational Site Rolla Missouri 65401 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Cherry Hill New Jersey 08003 —
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 Medford Oregon 97504 —
GSK Investigational Site Greenville South Carolina 29615 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Austin Texas 78750 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Waco Texas 76712 —

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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01147848, 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 18, 2017 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01147848 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →