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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 Jun 25, 2026, 11:01 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

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

Study identification

NCT ID
NCT01134042
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
587 participants

Conditions and interventions

Conditions

Interventions

  • Fluticasone Furoate/Vilanterol Inhalation Powder Drug
  • Fluticasone Furoate Inhalation Powder Drug
  • Fluticasone Propionate Inhalation Powder Drug
  • Placebo Inhalation Powder 1 Other
  • Placebo Inhalation Powder 2 Other

Drug · Other

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
May 31, 2010
Primary completion
Sep 30, 2011
Completion
Sep 30, 2011
Last update posted
Jan 10, 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 10, 2017 · Synced Jun 25, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01134042 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →