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Completed Phase 3 Interventional Results available

Clinical Study Evaluating Safety and Efficacy of Fluticasone Furoate and Fluticasone Propionate in People With Asthma

ClinicalTrials.gov ID: NCT01436110

Public ClinicalTrials.gov record NCT01436110. 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 21, 2026, 8:26 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, Placebo Controlled Multi-centre Study to Evaluate the Efficacy and Safety of Fluticasone Furoate Inhalation Powder and Fluticasone Propionate Inhalation Powder in the Treatment of Asthma in Adults and Adolescents Not Currently Treated With Inhaled Corticosteroids

Brief summary

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

A randomised, double-blind, double-dummy, placebo controlled multi-centre study to evaluate the efficacy and safety of fluticasone furoate inhalation powder and fluticasone propionate inhalation powder in the treatment of asthma in adults and adolescents not currently treated with inhaled corticosteroids

Study identification

NCT ID
NCT01436110
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
351 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
Sep 2011 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Sep 2012 (Actual)
Last update posted
Jan 9, 2017

2011 – 2012

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
20
Facility City State ZIP Site status
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Rolling Hills Estates California 90274 —
GSK Investigational Site Sacramento California 95819 —
GSK Investigational Site San Jose California 95117 —
GSK Investigational Site Aventura Florida 33180 —
GSK Investigational Site Clearwater Florida 33756 —
GSK Investigational Site Hialeah Florida 33016 —
GSK Investigational Site Orlando Florida 32811 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Bethesda Maryland 20814 —
GSK Investigational Site Columbia Missouri 65203 —
GSK Investigational Site Las Vegas Nevada 89119 —
GSK Investigational Site Brick New Jersey 08724 —
GSK Investigational Site Utica New York 13502 —
GSK Investigational Site Cincinnati Ohio 45242 —
GSK Investigational Site Orangeburg South Carolina 29118 —
GSK Investigational Site Corsicana Texas 75110 —
GSK Investigational Site El Paso Texas 79903 —
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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01436110, 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 9, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01436110 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →