Study identifier:D5890L00004
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A comparison of Symbicort® Single inhaler Therapy (Symbicort® 200 Turbuhaler® 1 inhalation b.i.d. plus as needed) & conventional best practice for the treatment of persistent asthma in adolescents & adults–a 26-week, randomised, open-label, parallel group, multicentre study
asthma
Phase 3
No
Budesonide/formoterol Turbuhaler
All
1300
Interventional
12 Years - Minutes
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
The purpose of this study is to compare Symbicort Single Inhaler treatment with the Best Conventional Practice in patients with persistent asthma
Location
Location
Aldergrove, BC, Canada
Location
Bolton, Ontario, Canada
Location
Brampton, ON, Canada
Arms | Assigned Interventions |
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