Ascending Dose Study of the Safety and Tolerability of Alirocumab (SAR236553/REGN727) in Japanese Healthy Volunteers
A Randomized, Double-Blind, Placebo-Controlled, Ascending Single-Dose Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered SAR236553 in Japanese Healthy Male Subjects
Primary Objective:
To assess the safety and tolerability of ascending single doses of subcutaneously (SC) administered alirocumab (SAR236553/REGN727) in Japanese healthy male subjects.
Secondary Objectives:
- To assess the pharmacodynamics effect of a single SC dose of alirocumab on serum low-density lipoprotein cholesterol (LDL-C) and other lipids and apolipoproteins such as total cholesterol, high-density lipoprotein cholesterol (HDL-C), non-high-density lipoprotein cholesterol, very low-density lipoprotein cholesterol, Triglycerides, Apolipoprotein B, Apolipoprotein A1 and Lipoprotein(a).
- To assess the Pharmacokinetic profile of a single SC dose of alirocumab.
- To assess the immunogenicity of a single SC dose of alirocumab.
研究概览
地位
条件
详细说明
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
学习地点
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-
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Tokyo、日本
- Sanofi-Aventis Administrative Office
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Healthy male subject, between 20 and 65 years inclusive.
- Body weight between 50.0 and 95.0 kg inclusive, body mass index between 18.0 and 30.0 kg/m² inclusive.
- Serum LDL-C levels >100 mg/dL
Exclusion Criteria:
- Subject indicated for the use of statins according to criteria in Adult Treatment Panel (ATP) III Guidelines as updated in 2004
- Significant concomitant illness or history of significant illness such as cardiac, renal, neurological, endocrinological, dermatological, metabolic or lymphatic disease, or any other illness or condition that would adversely affect the subject's participation in this study.
- History or presence of drug or alcohol abuse
- Smoking more than 5 cigarettes or equivalent in any 24 hour period.
- Any medication (including St John's Wort) within 14 days before the inclusion or within 5 times the elimination half-life or pharmacodynamic (PD) half-life of that drug, whichever the longest; any vaccination within the last 28 days.
- Positive reaction to any of the following tests: hepatitis B surface (HBs Ag) antigen, anti-hepatitis B core antibodies (anti-HBc Ab), anti-hepatitis C virus (anti-HCV) antibodies, human immunodeficiency virus (HIV) antigen and antibodies, syphilis.
- Elevated cholesterol due to a secondary cause such as hypothyroidism or alcohol.
- Presence or history of drug hypersensitivity
- Initiation of a new exercise routine or major change to a previous exercise routine within 4 weeks prior to Screening.
- Initiation of a new diet or major change to a previous diet within 4 weeks prior to Screening.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Cohort 1
Alirocumab dose 1 versus placebo
|
Pharmaceutical form: lyophilized formulation Route of administration: subcutaneous
其他名称:
Pharmaceutical form: lyophilized formulation Route of administration: Subcutaneous |
|
实验性的:Cohort 2
Alirocumab dose 2 versus placebo
|
Pharmaceutical form: lyophilized formulation Route of administration: subcutaneous
其他名称:
Pharmaceutical form: lyophilized formulation Route of administration: Subcutaneous |
|
实验性的:Cohort 3
Alirocumab dose 3 versus placebo
|
Pharmaceutical form: lyophilized formulation Route of administration: subcutaneous
其他名称:
Pharmaceutical form: lyophilized formulation Route of administration: Subcutaneous |
|
实验性的:Cohort 4
Alirocumab dose 4 versus placebo
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Pharmaceutical form: solution Route of administration: subcutaneous
其他名称:
Pharmaceutical form: solution Route of administration: subcutaneous |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
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Number of participants with Adverse Events
大体时间:106 days
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106 days
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次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Change in serum Low-Density Lipoprotein Cholesterol (LDL-C) from baseline to each visit.
大体时间:106 days
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106 days
|
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Change in ApolipoproteinB, ApolipoproteinA1 and Lipoprotein(a) from baseline to each visit.
大体时间:106 days
|
106 days
|
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Change in Total Cholesterol (T-C), High-Density Lipoprotein Cholesterol (HDL-C), Very Low-Density Lipoprotein Cholesterol (VLDL-C) and Triglycerides (TG) from baseline to each visit.
大体时间:106 days
|
106 days
|
合作者和调查者
赞助
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.
Alirocumab (Lyophilized formulation)的临床试验
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Nanfang Hospital, Southern Medical University尚未招聘
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Population Health Research Institute完全的ST 抬高型心肌梗死 | 血脂异常 | 高胆固醇血症 | 高脂血症 | 急性冠状动脉综合征 | 药物的生理作用加拿大
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University Medical Centre Ljubljana招聘中高胆固醇血症 | 动脉粥样硬化性心血管疾病 (ASCVD)斯洛文尼亚
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Westside Medical Associates of Los AngelesRegeneron Pharmaceuticals; University of Washington未知