Efficacy of Lapaquistat Acetate in Subjects With Hypercholesterolemia

Takeda

Status and phase: Terminated; Phase 2

Conditions: Hypercholesterolemia

Treatments: Drug: Lapaquistat acetate; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT00865228

TAK-475_201

U1111-1122-8404 (Registry Identifier)

Details and patient eligibility

About

The purpose of this study is to determine the role of time of dosing on the lipid-lowering effects of lapaquistat acetate, once daily (QD) or twice daily (BID), in subjects with hypercholesterolemia.

Full description

Dyslipidemias are a group of metabolic disorders produced by raised concentrations of lipoproteins, especially low-density lipoprotein cholesterol the lipoprotein that transports endogenous cholesterol from the liver to the peripheral tissues. Increased cholesterol and triglyceride levels lead to an increased risk of arteriosclerosis, the underlying cause of heart attack, strokes and peripheral vascular disease. Despite changes in lifestyle and the availability of potent lipid-lowering agents, cardiovascular disease continues to be the major cause of death in Western Europe and North America.

Lapaquistat acetate is being developed by Takeda for the treatment of hypercholesterolemia.

Enrollment: 224 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Females of childbearing potential who are sexually active must agree to use a medically accepted means of contraception, and can neither be pregnant nor lactating from Screening throughout the duration of the study.
• Has prior to Randomization a mean low-density lipoprotein cholesterol greater than or equal to 130 mg/dL and less than or equal to 220 mg/dL for 2 consecutive samples.
• Has prior to Randomization mean triglycerides less than 400 mg/dL for 2 consecutive samples.
• Is willing and able to comply with a standardized, therapeutic lifestyle change diet or equivalent.

Exclusion criteria

• Has an alanine aminotransferase or aspartate aminotransferase level greater than 2 times the upper limit of normal during the screening period.

• Has a serum creatinine greater than133 mmol/L during the screening period.

• Has a creatine phosphokinase greater than 3 times the upper limit of normal, identified during the screening period.

• Has active liver disease or jaundice.

• Has a history of cancer that has been in remission for less than 5 years prior to the first dose of study medication.

• Has an endocrine disorder, such as Cushing syndrome, hyperthyroidism, or inappropriately treated hypothyroidism, affecting lipid metabolism.

• Has a history of myocardial infarction, angina pectoris, unstable angina, transient ischemic attacks, cerebrovascular accident, peripheral vascular disease, abdomin al aorticaneurysm, coronary angioplasty, coronary or peripheral arterial surgery or multiple risk factors that confer a 10-year risk for cardiovascular disease greater than 20% based on Framingham risk scoring.

• Has a positive hepatitis B surface antigen, or antibody to hepatitis C virus, as determined by medical history and/or subject's verbal report.

• Has a positive human immunodeficiency virus status or is taking antiretroviral medications, as determined by medical history and/or subject's verbal report.

• Has received any investigational compound within 30 days prior to screening Visit 1, or is currently participating in another investigational study.

• Has received lapaquistat acetate in a previous clinical study or as a therapeutic agent.

• Has a history or presence of clinically significant food allergy that would prevent adherence to the specialized diet.

• Has a known heterozygous or homozygous familial hypercholesterolemia or known type III hyperlipoproteinemia.

• Has fibromyalgia, myopathy, rhabdomyolysis, or unexplained muscle pain.

• Has uncontrolled hypertension despite treatment at Screening Visit 1.

• Has had inflammatory bowel or any other malabsorption syndrome or has had gastric bypass or any other surgical procedure for weight loss.

• Has a history of drug abuse or alcohol abuse within the past 2 years.

• Has stage I squamous cell carcinoma of the skin.

• Has type 1 or type 2 diabetes mellitus.

• Is required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:

  • Fluvastatin
  • Lovastatin
  • bile acid sequestrants (eg, cholestyramine)
  • intestinal cholesterol uptake inhibitors (eg, ezetimibe)
  • Fibrates (eg, fenofibrate, gemfibrozil)
  • Niacin
  • Cholestin
  • red yeast rice
  • fish oils
  • plant sterols and stanols
  • orlistat
  • sibutramine
  • isotretinoin
  • tacrolimus
  • Probucol
  • Systemic corticosteroids and androgens
  • Potent CYP3A4 inhibitors
  • Cyclosporine
  • Erythromycin
  • Clarithromycin
  • Telithromycin
  • human immunodeficiency virus protease inhibitors
  • amiodarone
  • diltiazem
  • verapamil
  • nefazodone
  • grapefruit juice

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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224 participants in 4 patient groups, including a placebo group

Lapaquistat Acetate 100 mg QD (morning)

Experimental group

Treatment:

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Lapaquistat Acetate 100 mg QD (evening)

Experimental group

Treatment:

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Lapaquistat Acetate 50 mg BID

Experimental group

Treatment:

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Drug: Lapaquistat acetate

Placebo BID

Placebo Comparator group

Treatment:

Drug: Placebo