Study identifier:D3560L00068
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
Evaluation of the efficacy and safety of rosuvastatin 5 mg versus pravastatin 40 mg and atorvastatin 10 mg in subjects with type IIa and IIb hypercholesterolaemia
type IIa and IIb hypercholesterolaemia
Phase 4
No
Rosuvastatin, Pravastatin, Atorvastatin
All
668
Interventional
18 Years +
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Jun 2011 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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The purpose of this study is to evaluate the efficacy and safety of Rosuvastatin 5 mg as an hypercholesterolemia treatment comparatively at 2 other statins: Pravastatin 40 mg and Atorvastatin 10 mg. Treatment efficacy will be evaluated by the percentage of LDL-C variation after 8 weeks of treatment.
Location
Location
AIX EN PROVENCE, France
Location
ALLAIRE, France
Location
AMIENS, France
Location
ANCERVILLE, France
Location
ANGERS, France
Location
ANNECY, France
Location
ANZIN, France
Location
ARLES, France
Arms | Assigned Interventions |
---|---|
Active Comparator: 1 Rosuvastatin and Pravastatin | Drug: Rosuvastatin 5mg oral Other Name: Crestor Drug: Pravastatin 40mg oral Other Name: Prevachol |
Active Comparator: 2 Rosuvastatin and Atorvastatin | Drug: Rosuvastatin 5mg oral Other Name: Crestor Drug: Atorvastatin 10mg oral Other Name: Lipitor |
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