An Open-Label Extension Study to Evaluate the Safety and Tolerability of Lapaquistat Acetate in Subjects With Hypercholesterolemia

Takeda0 个研究点目标入组 574 人开始时间: 2005年12月最近更新: 2012年5月24日

适应症

干预措施

试验速览

阶段: 3 期
状态: 已完成
发起方
入组人数: 574
主要终点: Clinical Laboratory Serum Chemistries

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者记录与标识符相似试验

研究概览

简要总结

The purpose of this study is to determine the long-term safety of lapaquistat acetate, once daily (QD), as monotherapy or in combination with other lipid-lowering agents in Subjects with Hypercholesterolemia.

详细描述

Elevated plasma cholesterol (hypercholesterolemia) and various other plasma lipid imbalances (dyslipidemias) are major risk factors for coronary heart disease. Normally, the balance among cholesterol synthesis, dietary intake, and degradation is adequate to maintain healthy cholesterol plasma levels. However, in patients with hypercholesterolemia, elevation in low-density lipoprotein cholesterol leads to atherosclerotic deposition of cholesterol in the arterial walls. Consequently, it has been established that lowering the low-density lipoprotein cholesterol plasma concentration effectively reduces cardiovascular morbidity and mortality. As a result of this finding, the National Cholesterol Education Program Adult Treatment Panel III identifies control of low-density lipoprotein cholesterol as essential in the prevention and management of coronary heart disease. Additional lipid risk factors designated by Adult Treatment Panel III include elevated triglycerides, elevated non-high density lipoprotein cholesterol, and low levels of high-density lipoprotein cholesterol. Lipoproteins rich in triglycerides, such as very low-density lipoprotein cholesterol, appear to contribute to atherosclerosis, whereas the apparent protective effect of high-density lipoprotein cholesterol may be limited at low density lipoprotein concentrations.

Lapaquistat acetate is a squalene synthase inhibitor currently under development at Takeda for the treatment of dyslipidemia.

Participants in this study have primary hypercholesterolemia and have completed either the 12-week monotherapy protocol 01-04-TL-475-008 (NCT00143663) or the 24-week atorvastatin add-on study 01-04-TL-475-009 (NCT00143676).

研究设计

研究类型: Interventional
分配方式: Na
干预模型: Single Group
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Has completed the 01-04-TL-475-008 or 01-04-TL-475-009 study.
•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 clinical laboratory evaluations within reference range for the testing laboratory at the previous visit in study 01-04-TL-475-008 or 01-04-TL-475-009 unless the results were deemed not clinically significant by the investigator or sponsor.
•Is willing and able to comply with a standardized low cholesterol diet.
•Is willing to continue taking the protocol-specified companion lipid-altering medication from the previous study (if applicable) for at least the first 4 weeks.

排除标准

•Has an alanine aminotransferase or aspartate aminotransferase level greater than or equal to 3 times the upper limit of normal at the previous visit in the prior study, active liver disease, or jaundice.
•Has serum creatinine greater than or equal to 133 μmol/l at the previous visit in the prior study.
•Has a creatine kinase greater than or equal to 10 times the upper limit of normal at the previous visit in the prior study.
•Has a previous history of cancer that had been in remission for less than 5 years prior to the first dose of study medication. This criterion did not include those subjects with basal cell or Stage 1 squamous cell carcinoma of the skin.
•Has an endocrine disorder, such as Cushing's syndrome, hyperthyroidism, or inappropriately treated hypothyroidism, affecting lipid metabolism.
•Has a positive hepatitis B surface antigen, or hepatitis C virus antibody, as determined by medical history and/or participant's verbal report.
•Has a positive human immunodeficiency virus status or was taking antiretroviral medications, as determined by medical history and/or subject's verbal report.
•Has a known hypersensitivity to lapaquistat acetate.
•Has a history or presence of clinically significant food allergy that prevented them from maintaining Therapeutic Lifestyle Change (or equivalent) diet.
•Has a known homozygous familial hypercholesterolemia or known Type III hyperlipoproteinemia.
•Has fibromyalgia, myopathy, rhabdomyolysis, or unexplained muscle pain.
•Has uncontrolled hypertension at Visit
•Has inflammatory bowel disease or any other malabsorption syndrome or had gastric bypass or any other surgical procedure for weight loss.
•Has a history of drug abuse or a history of alcohol abuse within the past 2 years.
•Has any other serious disease or condition at Visit 1 that may reduce life expectancy, impair successful management according to the protocol, or make the participant unsuitable to receive study medication.
•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:
•Sibutramine
•Isotretinoin
•Tacrolimus
•Systemic corticosteroids and androgens
•Potent cytochrome P-450 3A4 inhibitors
•Azole antifungal agents
•Cyclosporine
•Erythromycin
•Clarithromycin
•Human Immunodeficiency Virus protease inhibitors
•Amiodarone
•Verapamil
•Diltiazem
•Nefazodone
•Large quantities of grapefruit juice

研究组 & 干预措施

Lapaquistat Acetate 100 mg QD

Experimental

干预措施: Lapaquistat acetate (Drug)

Lapaquistat Acetate 100 mg QD + Added Therapy

Experimental

干预措施: Lapaquistat acetate and additional lipid-lowering therapy (Drug)