Dyslipidemia Clinical Trial
Official title:
A Phase IIb, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Dose-Ranging Study to Assess the Efficacy and Safety of MK0859 in Japanese Patients With Dyslipidemia
This study will investigate the effect of MK0859 when administered alone and when in combination with atorvastatin in lowering Low Density Lipoprotein -Cholesterol (LDL-C) in Japanese patients with dyslipidemia.
This is the dose ranging study to evaluate efficacy and safety of MK-0859 in Japanese
patients.
Eligible patients were assigned to 1 of 10 treatment groups (including treatment groups with
or without administrative atorvastatin) for an 8-week treatment period which was followed by
a 8-week reversibility period.
As an additional follow-up, the pregnancy information from women of childbearing potential
who were treated with MK-0859 in this study will be collected retrospectively for a period
of 4 years after the last dose of MK-0859.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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