A Study of the Safety and Efficacy of Anacetrapib (MK-0859) When Added to Ongoing Statin Therapy (MK-0859-021 AM1)

Inclusion Criteria:

- If female, cannot be of reproductive potential

- Have been treated with an optimal dose of statin for at least 6 weeks

- Coronary heart disease (CHD) or other atherosclerotic vascular disease with multiple
risk factors (including diabetes, metabolic syndrome) and/or high LDL-C/low HDL-C, or
needing to meet a specific LDL-C/HDL-C goal

Exclusion Criteria:

- Previously participated in a study with a cholesteryl ester transfer protein (CETP)
inhibitor

- Homozygous familial hypercholesterolemia

- Severe chronic heart failure

- Uncontrolled cardiac arrhythmias, myocardial infarction (MI), percutaneous coronary
intervention (PCI), coronary artery by-pass graft (CABG), unstable angina, or stroke
within 3 months

- Uncontrolled hypertension

- Uncontrolled endocrine or metabolic disease known to influence serum lipids or
lipoproteins

- Active or chronic hepatobiliary, hepatic, or gall bladder disease

- History of mental instability, drug/alcohol abuse within the past five years or major
psychiatric illness inadequately controlled and unstable

- History of ileal bypass, gastric bypass, or other significant condition associated
with malabsorption

- Human immunodeficiency virus (HIV) positive

- History of malignancy ≤5 years

- Donated blood products or has had phlebotomy of >300 mL within 8 weeks or intends to
donate 250 mL of blood products or receive blood products within the projected
duration of the study

- Currently taking medications that are potent inhibitors or inducers of cytochrome
P450 3A4 (CYP3A) (including but not limited to cyclosporine, systemic itraconazole or
ketoconazole, erythromycin, clarithromycin, or telithromycin, nefazodone, protease
inhibitors, carbamazepine, phenobarbital, phenytoin, rifabutin, rifampin, St John's
wort) or has discontinued treatment <3 weeks prior

- Consumes more than 2 alcoholic drinks per day

- Currently participating or has participated in a study with an investigational
compound or device within 3 months

- Receiving treatment with systemic corticosteroids or taking systemic anabolic agents