A 26-week, double blind, randomised, mulit-centre, phase IIIb, parallel group study to compare the efficacy and safety of rosuvastatin (40 mg) with atorvastatin (80 mg) in subjects with hypercholesterolaemia and coronary heart disease or CHD risk equivalents.
Study identifier:4522IL/0103
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Study Complete
Official Title
A 26-week, double blind, randomised, mulit-centre, phase IIIb, parallel group study to compare the efficacy and safety of rosuvastatin (40 mg) with atorvastatin (80 mg) in subjects with hypercholesterolaemia and coronary heart disease or CHD risk equivalents.
Medical condition
hypercholesterolaemia
Phase
Phase 3
Healthy volunteers
-
Study drug
-
Sex
-
Actual Enrollment
-
Study type
Interventional
Age
-
Date
Study Start Date: 01 Jan 1971
Primary Completion Date: -
Study Completion Date: -
Study design
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verification:
-
Sponsors
AstraZeneca
Collaborators
-
Inclusion and exclusion criteria
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