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Clinical Trial Summary

ioequivalence study between two inhaler products of fixed dose combination of fluticasone propionate and salmeterol xinafoate inhalation powder


Clinical Trial Description

A bioequivalence study of a single dose of the fixed-dose combination of fluticasone propionate and salmeterol xinafoate inhalation powder administered from Fluticasone propionate 500 mcg and Salmeterol xinafoate 50 mcg inhalation powder/Respirent Pharmaceuticals (test-Τ) as 2 inhalations and ADVAIR DISKUS® 500/50 mcg inhalation powder/GSK (reference-R) in healthy volunteers under fasting conditions. The study will be one-center crossover, randomized, 2-period, 2-sequence (RT and TR), single dose, laboratory-blinded. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04546256
Study type Interventional
Source Respirent Pharmaceuticals Co Ltd.
Contact
Status Completed
Phase Phase 1
Start date September 1, 2020
Completion date December 31, 2020

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