drugset / Trial / NCT01537692

Clinical Study to Evaluate the Pharmacokinetics and Safety of BDP HFA Nasal Aerosol

NCT01537692

Phase 1 Completed 30 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedCrossoverOpen-label

Summary

The purpose of this study is to compare the systemic levels of beclomethasone 17 monopropionate (17 BMP - the active metabolite of BDP) after intranasal administration of BDP HFA with the systemic levels of 17 BMP after administration of orally inhaled BDP HFA in healthy volunteers.

Timeline

Start
2009-03
Primary completion
2009-04
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Subject beclomethasone dipropionate Other / unclassified 80 ug Intranasal
Subject beclomethasone dipropionate Other / unclassified 320 ug Intranasal

Indications