This study will evaluate the effects of anacetrapib (MK-0859) on low-density lipoprotein-cholesterol (LDL-C) when compared to placebo in Japanese participants with dyslipidemia when added to an existing statin-modifying therapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
307
Percent Change from Baseline in LDL-C (beta-quantification [BQ] method)
Time frame: Baseline and Week 24
Percentage of Participants who Experience at Least One Adverse Event (AE)
Time frame: 64 weeks
Percent Change from Baseline in High-density Lipoprotein-cholesterol (HDL-C)
Time frame: Baseline and Week 24
Percent Change from Baseline in Non-HDL-C
Time frame: Baseline and Week 24
Percent Change from Baseline in Apolipoprotein B (Apo-B)
Time frame: Baseline and Week 24
Percent Change from Baseline in Apolipoprotein A-I (Apo-A-I)
Time frame: Baseline and Week 24
Percent Change from Baseline in Lipoprotein(a) (Lp[a])
Time frame: Baseline and Week 24
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