Study identifier:4522AS/0004
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A randomised, double-blind, placebo controlled, crossover dose-ranging study to investigate the effect of rosuvastatin (CRESTOR®) on high density lipoprotein kinetics in patients with the metabolic syndrome
Metabolic Syndrome
Phase 3
Yes
Rosuvastatin
Male
15
Interventional
30 Years - 70 Years
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
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No locations available
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