Safety and Efficacy Study of Fluticasone Furoate/Vilanterol (FF/VI) Fixed Dose Combination (FDC) Compared to FF Alone in Subjects With Asthma

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A RANDOMISED, DOUBLE-BLIND, PARALLEL GROUP, MULTICENTRE, STRATIFIED, STUDY EVALUATING THE EFFICACY AND SAFETY OF ONCE DAILY FLUTICASONE FUROATE/VILANTEROL INHALATION POWDER COMPARED TO ONCE DAILY FLUTICASONE FUROATE INHALATION POWDER IN THE TREATMENT OF ASTHMA IN PARTICIPANTS AGED 5 TO 17 YEARS OLD (INCLUSIVE) CURRENTLY UNCONTROLLED ON INHALED CORTICOSTEROIDS.

Intervention/treatment:
BREOELLIPTA (FLUTICASONE-VILANTEROL)/ FLUTICASONE
Medical condition:
ASTHMA
Protocol code:
HZA107116
Control number:
208091
Status:
Closed
Approved:
August 28, 2017
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT03248128
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
5 Years to 17 Years
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
GSK Response Center
Organization
GlaxoSmithKline
Phone:
866-435-7343
Sponsor
GLAXOSMITHKLINE INC

Locations

GSK Investigational Site
Québec, G1V 4W2

Ontario

GSK Investigational Site
Brampton, Ontario, L6T 0G1
GSK Investigational Site
Windsor, Ontario, N8X2G1

Results

See the results from the trial NCT03248128. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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