Study identifier:D5252C00008
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 3, randomised, open-label, crossover study to compare HFA vs CFC pMDI formulations of budesonide on methacholine hyper-reactivity in patients with stable, persistent, mild to moderate asthma
asthma
Phase 3
No
Budesonide HFA, Budesonide CFC
All
99
Interventional
18 Years - 65 Years
Allocation: Randomized
Endpoint Classification: Bio-equivalence Study
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Oct 2012 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
-
No locations available
Arms | Assigned Interventions |
---|---|
Active Comparator: Budesonide Hydrofluoroalkane (HFA) 100 Budesonide Hydrofluoroalkane (HFA) 100 mcg twice daily for 2 weeks | Drug: Budesonide HFA standard daily inhaled dose |
Active Comparator: Budesonide HFA 400 Budesonide HFA 400 mcg twice daily for 2 weeks | Drug: Budesonide HFA standard daily inhaled dose |
Active Comparator: Budesonide Chlorofluorocarbon (CFC) 100 Budesonide Chlorofluorocarbon(CFC) 100 mcg twice daily for 2 weeks | Drug: Budesonide CFC standard daily inhaled dose |
Active Comparator: Budesonide CFC 400 Budesonide CFC 400 mcg twice daily for 2 weeks | Drug: Budesonide CFC standard daily inhaled dose |