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BE Study of Fluticasone Propionate/Salmeterol Inhalation Powder in Asthma Patients

Bronchial Asthma Clinical Trial

Official title:
A Multicenter, Randomized, Parallel-group, Placebo-controlled, 4-week Clinical Endpoint Bioequivalence Study Comparing Fluticasone Propionate/Salmeterol 100/50 µg Inhalation Powder With Advair® Diskus 100/50 µg in Asthma Patients

Clinical Trial Summary

The purpose of this study is to demonstrate the pharmacodynamic bioequivalence of the test product to the reference product in adult patients with asthma.

Clinical Trial Description

This study is to demonstrate the pharmacodynamic bioequivalence of the test product to the reference product in terms of FEV1 measured at different time-points in adult patients with asthma. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03394989
Study type Interventional
Source Cipla Ltd.
Contact
Status Completed
Phase Phase 3
Start date October 17, 2018
Completion date March 31, 2020
View Details
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