The primary objective of this study is to assess the effect of AVE5530 on LDL-C levels over a period of 4 weeks. The secondary objectives are to assess the effects of AVE5530 on other lipid plasma levels and the safety and tolerability of AVE5530.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
206
Sanofi-Aventis Administrative Office
Santiago, Chile
Sanofi-Aventis Administrative Office
Budapest, Hungary
Sanofi-Aventis Administrative Office
México, Mexico
Sanofi-Aventis Administrative Office
Moscow, Russia
Percent change in LDL-C from baseline
Time frame: 4 weeks
Absolute change from in LDL-C levels
Time frame: 4 weeks
Percent change in other lipids and lipoprotein fractions from baseline
Time frame: 4 weeks
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Sanofi-Aventis Administrative Office
Seoul, South Korea
Sanofi-Aventis Administrative Office
Istanbul, Turkey (Türkiye)