Study identifier:4522US/0001
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A 12-week randomized, open-label 3-arm, parallel group, multicenter Phase IIIb study comparing efficacy and safety of rosuvastatin 20mg and 40mg with that of atorvastatin 80 mg in subjects with acute coronary syndromes
Acute Coronary Syndromes
Phase 3
No
rosuvastatin calcium, atorvastatin
All
825
Interventional
18 Years - 70 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Dec 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
Arms | Assigned Interventions |
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