SB-659032 Platelet Aggregation Study
2012年12月6日 更新者:GlaxoSmithKline
A Double Blind Study to Evaluate Effects of Repeat Doses of SB-659032 on Platelet Aggregation in Healthy Volunteers
This study is designed to assess whether inhibition of plasma Lp-PLA2 activity impacts platelet function as assessed by ex vivo platelet aggregation tests and in vivo plasma biomarkers.
研究概览
详细说明
SB-659032 is a selective and orally active inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2) that is being developed for the treatment of atherosclerosis.
This study is designed to assess whether inhibition of plasma Lp-PLA2 activity impacts platelet function as assessed by ex vivo platelet aggregation tests and in vivo plasma biomarkers.
Blood samples for PK analysis and measurement of Lp-PLA2 activity will also be collected.
Questionnaires will be completed to evaluate the frequency of odorrelated AEs with non-enteric coated formulation of SB-659032 relative to placebo.
This will be a double blind, repeat dose, randomized, placebo-controlled, two period, period balanced, crossover study.
There will be a minimum of a 21 day washout period between dosing in each period.
研究类型
介入性
注册 (实际的)
26
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
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New South Wales
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Randwick, Sydney、New South Wales、澳大利亚、2031
- GSK Investigational Site
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 55年 (成人)
接受健康志愿者
是的
有资格学习的性别
男性
描述
Inclusion Criteria:
- Healthy adult males between 18 and 55 years of age, inclusive
- Body weight greater than 50 kg (110 pounds) and body mass index (BMI) between 19 and 32 where: BMI = weight in kg/(height in meters)2
- A signed and dated written informed consent prior to admission to the study
- The subject is able to understand and comply with protocol requirements, instructions and protocol-stated restrictions.
Exclusion Criteria:
- Any clinically relevant abnormality identified on the screening medical assessment, laboratory examination or ECG
- Platelet count below or above the reference range
- History of hypercoagulable state or history of thrombosis
- History of platelet dysfunction
- A known history of Gilbert's Syndrome
- History of asthma, anaphylaxis or anaphalactoid reactions, severe allergic responses
- A history of alcohol, substance or drug abuse within the last year or a positive alcohol breath test at screening or predose in each period. Abuse of alcohol is defined as an average weekly intake of greater than or equal to 21 units (male) or an average daily intake of greater than or equal to 3 units (male). 1 unit is equivalent to a 285mL glass of full strength beer or 425 mL schooner of light beer or 1 (30 mL) measure of spirits or 1 glass (100 mL) of wine
- Positive urine drug screen at screening or predose in each period
- History of use of tobacco or nicotine containing products within 6 months of screening or a positive urine cotinine at screening or exhaled carbon monoxide test at predose in each period
- Positive HIV, Hepatitis B or Hepatitis C at screening
- Use of aspirin, aspirin-containing products, non-steroidal anti-inflammatory agents or any antiplatelet medication within 14 days prior to Day -1 of the study (a list of these drugs will be reviewed with the subject at screening and provided to them to take home)
- Use of prescription (including hormone replacement therapy) or non-prescription drugs and vitamins within 7 days or 5 half-lives (whichever is longer) prior to Day -1 of the study. An exception is acetaminophen which is allowed at doses of ≤ 2g/day
- Use of dietary/herbal supplements including (but not limited to) St. John's wort, kava, ephedra (ma huang), gingko biloba, DHEA, yohimbe, saw palmetto, ginseng and red yeast rice within 14 days prior to Day -1 of the study
- Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) prior to dosing
- Consumption of grapefruit or grapefruit juice within 7 days prior to Day -1 of the study
- A history of cholecystectomy or biliary tract disease including a history of liver disease with elevated liver function tests of known or unknown etiology
- An unwillingness to abstain from sexual intercourse with pregnant or lactating women or an unwillingness to use a condom and another form of contraception (e.g., IUD, birth control pills taken by female partner, diaphragm with spermicide) if engaging in sexual intercourse with a woman who could become pregnant until discharge from the study
- Donation of blood in excess of 500 mL within 56 days or donation of blood in excess of 250 mL within 7 days prior to dosing
- Full ADP- and/or collagen-induced aggregation (greater than and equal to 40%) at all three concentrations of one or both agonists, as assessed within 6 months prior to first dose and at Day -1 of each period
- No ADP- or collagen-induced aggregation (less than 40%) at the highest concentration of either agonist, as assessed within 6 months prior to first dose and at Day -1 of each period
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
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:交叉作业
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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实验性的:SB-659032
250 mg non-enteric coated SB-659032
|
匹配的安慰剂
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安慰剂比较:Placebo
matched placebo QD for 14 days
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Platelet aggregation
大体时间:14 days
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Percent maximum platelet aggregation following ADP- and collagen-induced aggregation
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14 days
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Biomarkers of platelet aggregation
大体时间:14 days
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Urinary 11-dehydrothromboxane B2 and blood CD62 concentrations
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14 days
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Lp-PLA2 inhibition
大体时间:14 days
|
Lp-PLA2 activity, expressed in terms of percent inhibition relative to baseline
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14 days
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Clinical safety data
大体时间:14 days
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spontaneous adverse event reporting, 12-Lead ECG, vital signs, nursing/physician observation and safety and laboratory tests
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14 days
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Mean concentrations of SB-659032 and its major metabolite, SB-664601
大体时间:14 days
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SB-659032 and SB-664601 concentrations
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14 days
|
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Frequency and intensity of odor-related adverse events
大体时间:14 days
|
The frequency and intensity of odor-related adverse events as reported by subjects will be summarized
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14 days
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2005年7月1日
初级完成 (实际的)
2005年12月1日
研究完成 (实际的)
2005年12月1日
研究注册日期
首次提交
2012年12月6日
首先提交符合 QC 标准的
2012年12月6日
首次发布 (估计)
2012年12月10日
研究记录更新
最后更新发布 (估计)
2012年12月10日
上次提交的符合 QC 标准的更新
2012年12月6日
最后验证
2012年12月1日
更多信息
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