Effects of Ezetimibe on the Absorption of Oxidized Cholesterol

NCT ID: NCT00794677

Last Updated: 2021-03-09

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 26 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-06-30
• Study Completion Date: 2008-09-30

Brief Summary

The purpose of this study is to test the effects of Zetia™ (ezetimibe) 10 milligrams (mg) on the absorption of oxysterol into the blood following a meal containing oxysterol.

Detailed Description

There are a number of cholesterol-lowering drugs available that can lower blood cholesterol to a healthier level. Zetia™ (ezetimibe) 10 mg is available by prescription for the treatment of high cholesterol. While Zetia has been shown to inhibit the absorption of dietary cholesterol into the bloodstream, its effects on oxysterol absorption from the diet have not been completely evaluated.

Conditions

Hypercholesterolemia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: TRIPLE

Study Groups

Sugar Pill

Placebo medication will be taken orally once daily in the morning on rising either during the first intervention period or the second intervention period. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

Blinded study medication (matched placebo) will be taken orally once daily in the morning on rising. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

ezetimibe

10 mg medication will be taken orally once daily in the morning on rising either during the first intervention period or the second intervention period. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

Group Type: EXPERIMENTAL

ezetimibe

Intervention Type: DRUG

Blinded study medication (ezetimibe 10 mg in tablet form) will be taken orally once daily in the morning on rising. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

Interventions

ezetimibe

Blinded study medication (ezetimibe 10 mg in tablet form) will be taken orally once daily in the morning on rising. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

Intervention Type: DRUG

placebo

Blinded study medication (matched placebo) will be taken orally once daily in the morning on rising. Single-blind ezetimibe placebo will be taken during the Run-In Period. Patients will be issued one bottle containing either active drug or placebo for each treatment period.

Intervention Type: DRUG

Other Intervention Names

Zetia; Sugar Pill

Eligibility Criteria

Inclusion Criteria

• Not currently pregnant or lactating and is highly unlikely to conceive
• Body Mass Index (BMI) between 20-30 kilograms per meter squared (kg/m2) inclusive.
• Body weight, as reported by patient, stable (±2 kg) for >6 weeks
• Plasma low density lipoprotein cholesterol (LDL-C) between 130 and 180 milligrams per deciliter (mg/dL) inclusive. Note: One retest allowed.
• Triglyceride (TG) concentrations ≤150 mg/dL. Note: One retest allowed.
• Fasting blood glucose <110 mg/dL and hemoglobin A1c (HbA1C) ≤ 6 percent at Visit 1. Note: One retest allowed.
• Liver transaminases (ALT, AST) ≤1.5 x upper limit of normal (ULN) and no active liver disease. Note: One retest allowed.
• Creatine Phosphokinase (CPK) ≤2x ULN. Note: One retest allowed.
• Willingness to maintain a stable diet for the duration of the study.
• Can understand and comply with study procedures and signs a written informed consent.
• Patient is ≥80 precent compliant with dosing during Placebo Run-In Period or, in the opinion of the investigator, is able to maintain ≥80 percent therapy compliance during the active treatment period of the study.

Exclusion Criteria

• Lipid-lowering therapy and replacement of this therapy with study medication is considered inappropriate by the investigator.
• Consumes an average of more than 2 alcoholic drinks per day.
• Smokes.
• Currently engages in a vigorous exercise regimen or intensive exercise bouts >4x per month.
• Treated with any other investigational drug within 30 days of Visit 1.
• Hypersensitivity or intolerance to ezetimibe or any component of this medication.
• Any condition or situation which poses a risk to the patient or interfere with participation in the study.
• Congestive heart failure.
• Uncontrolled cardiac arrhythmias.
• History of myocardial infarction, stroke, or any other clinical manifestation of coronary, cerebral, or peripheral vascular disease.
• Uncontrolled hypertension
• Impaired renal function, nephrotic syndrome or other clinically significant renal disease at Visit 1.
• Active or chronic hepatobiliary or hepatic disease.
• History of irritable bowel syndrome, ileal bypass, gastric bypass or any gastrointestinal disorder/condition associated with malabsorption.
• Uncontrolled endocrine or metabolic disease known to influence serum lipids or lipoproteins.
• Type I or Type II diabetes mellitus.
• Disorders of the hematologic, digestive, or central nervous systems including cerebrovascular disease and degenerative disease that would limit study evaluation or participation.
• Human Immunodeficiency Virus (HIV) positive.
• History of cancer within the past 5 years (except for successfully treated basal and squamous cell carcinomas).
• History of uncontrolled psychiatric illness or drug/alcohol abuse within the past 5 years. Individuals with psychiatric illness adequately controlled and stable on pharmacotherapy may be enrolled at the discretion of the investigator.
• Lipid-lowering agents taken within 6 weeks and fibrates taken within 8 weeks prior to visit 3.
• Cardiovascular medications are acceptable provided the patient has been on a stable regimen for at least 6 weeks prior to Visit 3 and indicates a willingness to continue the stable regimen for the duration of the study.
• Supplementation with antioxidants beyond a standard multivitamin for the duration of the study.
• Psyllium, other fiber-based laxatives, and/or over the counter (OTC) therapies known to affect serum lipid levels taken within 6 weeks of Visit 3.
• Female patients receiving hormone replacement therapy, any estrogen antagonist/agonist or hormonal contraceptives.
• Treatment with cyclosporine except for ophthalmic indication
• Anti-obesity medications such as orlistat or sibutramine taken within 3 months prior to Visit 1.
• Therapeutic doses of systemic corticosteroids except inhaled steroid therapy (for example, Pulmicort®) maintained on a stable dosing regimen for at least 6 weeks prior to randomization (Visit 3) and throughout the duration of the study

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Merck Schering-Plough

UNKNOWN

Sponsor Role: collaborator

UCSF Benioff Children's Hospital Oakland

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ronald M Krauss, M.D.

Role: PRINCIPAL_INVESTIGATOR

UCSF Benioff Children's Hospital Oakland

Locations

Cholesterol Research Center

Berkeley, California, United States

Countries

United States

Other Identifiers

MM6997

Identifier Type: -

Identifier Source: org_study_id