Study identifier:BY9010/M1-125
ClinicalTrials.gov identifier:NCT00546520
EudraCT identifier:N/A
CTIS identifier:N/A
A 3-period double-blind, cross-over study on the onset of action of inhaled ciclesonide (7 days of 400 mcg sid versus 800 mcg bid versus placebo) on airway responsiveness to adenosine monophosphate (AMP), sputum eosinophiles and exhaled breath nitric oxide (NO) in patients with asthma
asthma
Phase 3
No
Ciclesonide
All
21
Interventional
18 Years - 45 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind
Primary Purpose: Prevention
Verified 01 Feb 2017 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|