Efficacy and Safety Study of FP MDPI Compared With FS MDPI in Adolescent and Adult Patients With Persistent Asthma

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A 12-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED, EFFICACY AND SAFETY STUDY OF FLUTICASONE PROPIONATE MULTIDOSE DRY POWDER INHALER COMPARED WITH FLUTICASONE/SALMETEROL MULTIDOSE DRY POWDER INHALER IN ADOLESCENT AND ADULT PATIENTS WITH PERSISTENT ASTHMA SYMPTOMATIC DESPITE INHALED CORTICOSTEROID THERAPY

Intervention/treatment:
FLUTICASONE-SALMETEROL
Medical condition:
ASTHMA
Protocol code:
FSS-AS-30017
Control number:
175690
Status:
Closed
Approved:
July 17, 2014
Date Completed:
Trial phase:
Phase 3
For more information:
ClinicalTrials.gov - NCT02141854
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
12 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Director, Clinical Research
Organization
Teva Branded Pharmaceutical Products, R&D Inc.
Phone:
215-591-3000
Sponsor
TEVA BRANDED PHARMACEUTICAL PRODUCTS R&D INC

Locations

Ontario

Teva Investigational Site 11072
Toronto, Ontario

Quebec

Teva Investigational Site 11075
Vancouver, Quebec

Results

See the results from the trial NCT02141854. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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