Study identifier:BY9010/M1-413
ClinicalTrials.gov identifier:NCT00384475
EudraCT identifier:N/A
CTIS identifier:N/A
A randomized, double-blind, placebo-controlled, parallel-group study using the Environmental Exposure Chamber (EEC) to assess the Onset of Action of Ciclesonide, applied as a Nasal Spray (200 mcg, once daily), in the treatment of Seasonal Allergic Rhinitis (SAR) in patients 18 years and older
Rhinitis, Allergic, Seasonal
Phase 3
No
Ciclesonide Nasal Spray
All
500
Interventional
18 Years +
Allocation: Randomized 
Endpoint Classification: None 
Intervention Model: Parallel Assignment 
Masking: Double Blind 
Primary Purpose: Treatment 
Verified 01 Oct 2016 by AstraZeneca
AstraZeneca
-
No locations available
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