12-week Open-label, Phase IIIb Comparing Efficacy and Safety of Rosuvastatin (CRESTOR™) in Combination with Ezetimibe - GRAVITY

Study identifier:D356FC00003

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A 12-week Open-label, Randomised, Parallel-group, Multicentre, Phase IIIb Study to Compare the Efficacy and Safety of Rosuvastatin (CRESTOR™) in Combination with Ezetimibe and Simvastatin in Patients with Hypercholesterolaemia and CHD

Medical condition

Hypercholesterolemia

Phase

Phase 3

Healthy volunteers

No

Study drug

Rosuvastatin (Crestor), Ezetimibe, Simvastatin

Sex

All

Actual Enrollment

1743

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 01 Aug 2007
Primary Completion Date: 01 Sept 2008
Study Completion Date: 01 Sept 2008

Study design

Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment

Verification:

Verified 01 May 2011 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria