drugset / Trial / NCT01537692
Clinical Study to Evaluate the Pharmacokinetics and Safety of BDP HFA Nasal Aerosol
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | beclomethasone dipropionate | Other / unclassified | 80 ug | Intranasal |
| Subject | beclomethasone dipropionate | Other / unclassified | 320 ug | Intranasal |