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Completed Phase 3 Interventional Results available

A 12-Week Study To Assess The Safety Of Fluticasone Propionate/Salmeterol 100/50 Hydrofluoroalkane (HFA) Versus Fluticasone Propionate 100 HFA In Children With Asthma

ClinicalTrials.gov ID: NCT00441441

Public ClinicalTrials.gov record NCT00441441. 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 Sep 2, 2026, 9:46 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

A Randomized, Double-blind, Parallel Group Study Evaluating the Safety of Fluticasone Propionate/Salmeterol 100/50mcg HFA (2 Inhalations of 50/25mcg) Twice Daily Compared With Fluticasone Propionate 100mcg HFA (2 Inhalations of 50mcg) Twice Daily in Subjects 4-11 Years of Age With Persistent Asthma

Brief summary

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

This study is to assess the safety of an investigational drug in children 4 to 11 years of age who have asthma. The subjects will attend 7 clinic visits, of which up to 3 will be in the morning, and have lung function tests performed.

Study identification

NCT ID
NCT00441441
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
4 Years to 11 Years
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
Jan 31, 2007
Primary completion
Dec 31, 2007
Completion
Dec 31, 2007
Last update posted
Dec 15, 2016

2007 – 2008

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
GSK Investigational Site Huntington Beach California 92647
GSK Investigational Site Long Beach California 90806
GSK Investigational Site Long Beach California 90808
GSK Investigational Site Riverside California 92506
GSK Investigational Site Denver Colorado 80206
GSK Investigational Site Lakewood Colorado 80401
GSK Investigational Site Jacksonville Florida 32207
GSK Investigational Site Gainesville Georgia 30501
GSK Investigational Site Ypsilanti Michigan 48197
GSK Investigational Site Cortland New York 14850
GSK Investigational Site Raleigh North Carolina 27607
GSK Investigational Site Canton Ohio 44718
GSK Investigational Site Oklahoma City Oklahoma 73120
GSK Investigational Site Lake Oswego Oregon 97035
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Portland Oregon 97213
GSK Investigational Site Pittsburgh Pennsylvania 15241
GSK Investigational Site Charleston South Carolina 29407
GSK Investigational Site Germantown Tennessee 38138
GSK Investigational Site South Burlington Vermont 05403

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 35 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00441441, 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 Dec 15, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00441441 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →