Study identifier:BY9010/M1-131
ClinicalTrials.gov identifier:NCT00163345
EudraCT identifier:N/A
CTIS identifier:N/A
Evaluation of parameters of the small airways and their changes under treatment with ciclesonide (320 mcg once daily) versus placebo in patients with asthma
asthma
Phase 3
No
Ciclesonide
All
20
Interventional
18 Years - 60 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Dec 2016 by AstraZeneca
AstraZeneca
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The aim of this study is to evaluate the involvement of small airways in asthma, as determined by bronchial challenges, CT-scanning, and cellular markers of inflammation. Ciclesonide will be inhaled at one dose level once daily. The study duration consists of a baseline period (2 to 3 weeks) and a treatment period (5 to 6 weeks). The study will provide further data on safety and tolerability of ciclesonide.
Location
Location
RB Groningen, Netherlands, 9700
Arms | Assigned Interventions |
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