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Clinical Trial Summary

Τherapeutic equivalence, randomized, multiple-dose, placebo-controlled, observer-blind, parallel group design consisting of a 2-week run-in period followed by a 4-week treatment period with Fluticasone propionate 100 mcg and Salmeterol 50 mcg inhalation powder/Respirent Pharmaceuticals (Test) or ADVAIR DISKUS® 100/50 mcg (Reference) or placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05664061
Study type Interventional
Source Respirent Pharmaceuticals Co Ltd.
Contact Chrysoula Doxani, MD, MSc, PhD
Phone +30 2410257310
Email doxani@becro.gr
Status Recruiting
Phase Phase 3
Start date January 30, 2023
Completion date December 31, 2023

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