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Completed Phase 3 Interventional Results available

Study HZA106829: Efficacy/Safety Study of Fluticasone Furoate/Vilanterol (GW642444) in Adult and Adolescent Asthmatics

ClinicalTrials.gov ID: NCT01134042

Public ClinicalTrials.gov record NCT01134042. 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, 12:33 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

HZA106829: A Randomised, Double-blind, Parallel Group, Multicentre Study of Fluticasone Furoate/GW642444 Inhalation Powder, Fluticasone Furoate Inhalation Powder Alone, and Fluticasone Propionate Alone 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 each evening with fluticasone furoate inhalation powder administered alone once daily each evening in adolescent and adult subjects 12 years of age and older with persistent bronchial asthma over a 24-week period.

Study identification

NCT ID
NCT01134042
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
587 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
Oct 2011 (Actual)
Completion
Oct 2011 (Actual)
Last update posted
Jan 11, 2017

2010 – 2011

United States locations

U.S. sites
23
U.S. states
10
U.S. cities
22
Facility City State ZIP Site status
GSK Investigational Site Bell Gardens California 90201 —
GSK Investigational Site Huntington Beach California 92647 —
GSK Investigational Site Long Beach California 90808 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Roseville California 95661 —
GSK Investigational Site San Diego California 92128 —
GSK Investigational Site Clearwater Florida 33756 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Panama City Florida 32405 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Normal Illinois 61761 —
GSK Investigational Site River Forest Illinois 60305 —
GSK Investigational Site Asheville North Carolina 28801 —
GSK Investigational Site Cincinnati Ohio 45231 —
GSK Investigational Site Oklahoma City Oklahoma 73103 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Lake Oswego Oregon 97035 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Austin Texas 78756 —
GSK Investigational Site El Paso Texas 79925 —
GSK Investigational Site Sugar Land Texas 77479 —

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 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01134042, 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 11, 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 NCT01134042 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →