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Clinical Trial Summary

The purpose of this study is to evaluate the onset of action of fluticasone propionate nasal spray compared to placebo nasal spray in reducing nasal allergic signs and symptoms following ragweed exposure in the Allergen BioCube (ABC) after up to 14 days of at home dosing.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01439815
Study type Interventional
Source ORA, Inc.
Contact
Status Completed
Phase Phase 4
Start date September 2011
Completion date October 2011

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