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Clinical Trial Summary

The primary objective of the study is to compare nighttime symptom relief of fluticasone furoate nasal spray versus oral fexofenadine


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00502775
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date August 2007
Completion date November 2007

See also
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