Safety and Pharmacokinetics of BIRB 796 BS Tablets Administered to Healthy Human Subjects
2014年8月5日 更新者:Boehringer Ingelheim
Safety and Pharmacokinetics of BIRB 796 BS Tablets Administered Twice Daily Orally (Total Daily Dose 30, 60, and 120 mg) to Healthy Human Subjects for 14 Days. A Double-blind, Placebo-controlled, Parallel Group Study.
Study to assess the safety and pharmacokinetics of BIRB 796 BS tablets administered as multiple daily doses at various dose levels.
研究概览
研究类型
介入性
注册 (实际的)
49
阶段
- 阶段1
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 45年 (成人)
接受健康志愿者
不
有资格学习的性别
男性
描述
Inclusion Criteria:
- Healthy male subjects as determined by results of screening
- Signed written informed consent in accordance with Good Clinical Practice and local legislation
- Age >= 18 and <= 45 years
- Broca >= - 20 % and <= + 20%
- Able to communicate well with the investigator and to comply with study requirements
- > 10 elimination half lives present since last use of any investigational drug for that investigational drug
- Laboratory values within a clinically relevant reference range
Exclusion Criteria:
- Any finding of the medical examination (including blood pressure, pulse rate, temperature, and EKG) deviating from normal and of clinical relevance
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Surgery of gastrointestinal tract (except appendectomy)
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- History of vasculitis (past history of fever, malaise, myalgias, rash, etc.)
- Intake of drugs with a long half-life (> 24 hours) (< 1 month prior to administration or during the trial)
- Use of any drugs, which might influence the results of the trial, (< 10 days prior to administration or during the trial)
- Participation in another trial with an investigational drug (< 1 months prior to administration or during trial)
- Smoker
- Inability to refrain from smoking on trial days
- Alcohol abuse (> 60 g/day)
- Drug abuse
- Use of methylxanthine-containing drinks or foods (coffee, tea, cola, energy drinks, chocolate, etc.) < one week prior to administration of study drug
- Blood donation or loss > 400 mL (< 1 month prior to administration or during the trial)
- Excessive physical activities (< 5 days prior to administration or during the trial)
- Following specific laboratory findings: total white blood cell >= 10 x 109/L, C-Reactive Protein >= 4.5 mg/L, gamma-glutamyl-transferase >= 25 U/L, aspartate transaminase >= 16 U/L, alanine transaminase >= 20 U/L any erythrocytes or > 15 mg/dl protein on urine dipstick
- Any EKG value outside of the reference range of clinical relevance including, but not limited to QTcB > 480 ms, PR interval > 240 ms, QRS interval > 110 ms
- History of any familial bleeding disorder
- Inability to comply with dietary regimen of study centre
- Inability to comply with investigator's instructions
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 |
|---|---|
|
安慰剂比较:安慰剂
|
|
|
实验性的:BIRB 796 BS,低剂量
|
|
|
实验性的:BIRB 796 BS,高剂量
|
|
|
实验性的:BIRB 796 BS, medium dose
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
发生不良事件的患者人数
大体时间:最多 24 天
|
最多 24 天
|
|
Number of patients with clinically significant changes in vital signs
大体时间:up to 21 days
|
up to 21 days
|
|
Number of patients with clinically significant changes in laboratory parameters
大体时间:up to 21 days
|
up to 21 days
|
|
Number of patients with abnormal findings in electrocardiogram
大体时间:up to 21 days
|
up to 21 days
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Maximum concentration of the analyte in plasma (Cmax) for several time points
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Area under the plasma concentration versus time curve (AUC) for several time points
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Time at which maximum plasma concentration occurred over a dosing interval (tmax)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Terminal elimination rate constant (λZ)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Elimination half-life (t1/2)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Mean residence time (MRT)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Apparent oral clearance (CL/F)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
|
Apparent volume of distribution during the terminal elimination phase, divided by F (bioavailability factor) (Vz/F)
大体时间:up to 36 hours after dosing
|
up to 36 hours after dosing
|
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。
有用的网址
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
2001年1月1日
初级完成 (实际的)
2001年3月1日
研究注册日期
首次提交
2014年8月5日
首先提交符合 QC 标准的
2014年8月5日
首次发布 (估计)
2014年8月6日
研究记录更新
最后更新发布 (估计)
2014年8月6日
上次提交的符合 QC 标准的更新
2014年8月5日
最后验证
2014年8月1日
更多信息
与本研究相关的术语
其他研究编号
- 1175.14
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