Study identifier:BY9010/M1-137
ClinicalTrials.gov identifier:NCT00163397
EudraCT identifier:N/A
CTIS identifier:N/A
A comparative study of inhaled ciclesonide 160 mcg/day vs budesonide 400 mcg/day in patients with asthma
asthma
Phase 3
No
Ciclesonide
All
120
Interventional
18 Years - 75 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Oct 2016 by AstraZeneca
AstraZeneca
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The aim of the study is to investigate the efficacy of ciclesonide versus budesonide on lung function, symptoms and use of rescue medication in patients with asthma. Ciclesonide and budesonide will be inhaled once daily at one dose level each. The study duration consists of a baseline period (1 to 4 weeks) and a treatment period (12 weeks). The study will provide further data on safety and tolerability of ciclesonide.
Location
Location
Kota Bharu / Kelantan, Malaysia, 16150
Location
Kuala Lumpur, Malaysia, 50586
Location
Kuala Lumpur, Malaysia, 50603
Location
Kuala Lumpur, Malaysia, 56000
Location
Taipei, Taiwan, Province of China
Location
Taipei City 114, Taiwan, Province of China, 886-114
Arms | Assigned Interventions |
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