Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42165279 in Healthy Young and Elderly Participants
2014年12月2日 更新者:Janssen Research & Development, LLC
A Double-Blind, Placebo-Controlled, Randomized, Multiple Dose Study to Investigate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of JNJ-42165279 in Healthy Young and Elderly Subjects
The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of JNJ-42165279 in healthy, young and elderly, male and female participants after repeated oral dose administration.
研究概览
详细说明
This is a double-blind (neither physician nor participant knows the treatment that the participant receives), randomized (the study drug is assigned by chance), placebo-controlled (an inactive substance is compared with a medication to test whether the medication has a real effect in a clinical study) trial that will be conducted in two parts.
Thirty two (32) healthy participants are planned to be included in total, in four cohorts (groups).
Participants in each cohort will receive JNJ-42165279 (n=6) or placebo (n=2) once-daily for 10 consecutive days.
In Part 1, two cohorts of healthy male participants, 18 to 55 years of age, will be enrolled.
Cohort A will receive 50 mg JNJ-42165279 or placebo for 10 days, and Cohort B will receive 30 mg JNJ-42165279 or placebo for 10 days.
In Part 2, Cohort C will consist of 8 healthy female participants of non-childbearing potential (surgically sterile or postmenopausal), 18 to 58 years of age, who will receive 100 mg JNJ-42165279 or placebo for 10 days.
Cohort D will consist of 8 healthy elderly male or female participants, from 65 to 85 years of age, who will receive 100 mg JNJ-42165279 or placebo for 10 days.
The dose may be adapted before each cohort starts based on available data.
The maximum dose will not exceed 100 mg once-daily.
For all participants, this study will consist of an eligibility screening examination (between 28 and 3 days prior to the first dose administration), a double-blind treatment phase consisting of 2 days before dosing, 10 dosing days (Day 1 to 10), 4 days after dosing (Day 11 to 14), and a follow-up examination (within 7 to 14 days after last dose administration).
The total study duration for each participant will not exceed 8 weeks.
研究类型
介入性
注册 (实际的)
40
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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Merksem、比利时
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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 85年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Body Mass Index (BMI) between 18 and 30 kg/m2 inclusive
- Nonsmoker
- Healthy men between 18 and 55 years, inclusive (Cohorts A and B)
- Healthy women between 18 and 58 years, inclusive (Cohort C)
- Healthy men and women between 65 and 85 years of age, inclusive (Cohort D)
- Men who are sexually active with a woman of childbearing potential and have not had a vasectomy must agree to use a barrier method of birth control during the study and for 3 months after receiving the last dose of study drug. In addition, their female partners should also use an appropriate method of birth control for at least the same duration (Cohorts A, B, and D)
- Not be of childbearing potential due to either tubal ligation or hysterectomy, or who are postmenopausal (Cohorts C and D)
Exclusion Criteria:
- Clinically significant abnormal values for hematology, clinical chemistry or urinalysis at screening or admission
- Clinically significant abnormal physical examination, vital signs or electrocardiogram at screening or admission
- History of, or current, significant medical illness including (but not limited to) cardiac disease, hematological disease, lipid abnormalities, respiratory disease, diabetes mellitus, renal or hepatic insufficiency, thyroid disease, Parkinson's disease, infection, or any other illness that the Investigator considers should exclude the participant
- History of epilepsy or fits or unexplained black-outs
- Cohorts A and B only: a contraindication for spinal puncture
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: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 A (Part 1)
Healthy male participants, 18 to 55 years of age.
|
JNJ-42165279 50 mg orally administered once daily for 10 days.
Matching placebo orally administered once daily for 10 days.
|
|
实验性的:Cohort B (Part 1)
Healthy male participants, 18 to 55 years of age.
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Matching placebo orally administered once daily for 10 days.
JNJ-42165279 30 mg orally administered once daily for 10 days.
|
|
实验性的:Cohort C (Part 2)
Healthy female participants of nonchildbearing potential (surgically sterile or postmenopausal), 18 to 58 years of age.
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Matching placebo orally administered once daily for 10 days.
JNJ-42165279 100 mg orally administered once daily for 10 days.
|
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实验性的:Cohort D (Part 2)
Healthy elderly male or female participants, from 65 to 85 years of age.
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Matching placebo orally administered once daily for 10 days.
JNJ-42165279 100 mg orally administered once daily for 10 days.
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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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Plasma concentrations of JNJ-42165279
大体时间:2 weeks
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2 weeks
|
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Urine concentrations of JNJ-42165279
大体时间:2 weeks
|
2 weeks
|
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Concentrations in cerebrospinal fluid of JNJ-42165279
大体时间:2 weeks
|
2 weeks
|
|
The number of participants with adserve events as a measure of safety and tolerability
大体时间:Approximately 8 weeks
|
Approximately 8 weeks
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次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Enzyme fatty acid amide hydrolase inhibition, as measured in white blood cells (WBCs)
大体时间:Approximately 4 weeks
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Approximately 4 weeks
|
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Plasma concentrations of N-arachidonoylethanolamine (anandamide)
大体时间:2 weeks
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2 weeks
|
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Plasma concentrations of palmitoylethanolamide
大体时间:2 weeks
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2 weeks
|
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Plasma concentrations of oleoylethanolamide
大体时间:2 weeks
|
2 weeks
|
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Serum concentrations of prolactin
大体时间:10 days
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10 days
|
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Saliva concentrations of cortisol
大体时间:10 days
|
10 days
|
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Concentrations in cerebrospinal fluid of N-arachidonoylethanolamine (anandamide) or its metabolites
大体时间:9 days
|
9 days
|
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Concentrations in cerebrospinal fluid of palmitoylethanolamide or its metabolites
大体时间:9 days
|
9 days
|
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Concentrations in cerebrospinal fluid of oleoylethanolamide or its metabolites
大体时间:9 days
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9 days
|
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。
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
2013年10月1日
初级完成 (实际的)
2014年10月1日
研究完成 (实际的)
2014年10月1日
研究注册日期
首次提交
2013年10月14日
首先提交符合 QC 标准的
2013年10月14日
首次发布 (估计)
2013年10月17日
研究记录更新
最后更新发布 (估计)
2014年12月3日
上次提交的符合 QC 标准的更新
2014年12月2日
最后验证
2014年12月1日
更多信息
与本研究相关的术语
关键字
其他相关的 MeSH 术语
其他研究编号
- CR102575
- 42165279EDI1002 (其他标识符:Janssen Research & Development, LLC)
- 2013-002309-67 (EudraCT编号)
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.