Safety, Tolerance, and Pharmacokinetics of Single Rising Oral Doses of BILB 1941 ZW Solution in Healthy Male Subjects, Followed With Bioavailability Comparison of BILB 1941 ZW Tablet and Solution Formulation Administered With or Without Food
2014年10月2日 更新者:Boehringer Ingelheim
Safety, Tolerance, and Pharmacokinetics of Single Oral Doses of 5 mg, 20 mg, 60 mg, 120 mg, 200 mg, 300 mg, 600 mg, 1000 mg, 1500 mg, 2000 mg, 2400 mg, and 3000 mg BILB 1941 ZW (PEG 400/TRIS Solution) in Healthy Male Subjects, in a Randomised Double Blind, Placebo Controlled Rising Dose Study, Followed With an Open-label Intra-subject Three-Way Crossover Bioavailability Comparison of 600 mg BILB 1941 ZW in a PEG 400/TRIS Solution and 600 mg BILB 1941 ZW Tablet and 600 mg BILB 1941 ZW Tablet Administered With Food
The objective of the current study was to investigate the safety, tolerability, and pharmacokinetics of BILB 1941 ZW following the administration of single rising doses from 5 mg to 300 mg.
In addition the bioavailability of the 60 mg dose given fasted and after a high-fat breakfast was to be be investigated
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
56
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 50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 males according to the following criteria based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory tests:
1.1 No finding deviating from normal and of clinical relevance
1.2 No evidence of a clinically relevant concomitant disease
- Age ≥18 and Age ≤50 years, BMI ≥18.5 and BMI ≤29.9 kg/m2 (Body Mass Index)
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice (GCP) and the local legislation
Exclusion Criteria:
- Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders, including a clinical history of viral hepatitis, or serological evidence of active Hepatitis B or Hepatitis C infection
- History of orthostatic hypotension, fainting spells and blackouts
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
- Use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within 1 month prior to administration or during the trial
- Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on trial days
- Alcohol abuse (> 60 g/day)
- Drug abuse
- Blood donation of more than 100 mL within 1 month prior to administration or during the trial
- Excessive physical activities within 5 days prior to administration or during the trial
- Any laboratory value outside the clinically accepted reference range and of clinical relevance
- History of any familial bleeding disorder
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 |
|---|---|
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实验性的:BILB 1941 ZW - single rising dose
Single rising dose part
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安慰剂比较:Placebo
Single rising dose part
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实验性的:BILB 1941 ZW - tablet - fasted
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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实验性的:BILB 1941 ZW - solution
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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实验性的:BILB 1941 ZW - tablet - fed
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
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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 |
|---|---|---|
|
Number of subjects with abnormal findings in physical examination
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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Number of subjects with abnormal changes in laboratory parameters
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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Number of subjects with clinically significant changes in vital signs
大体时间:up to 48 hours following drug administration
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Blood pressure, Pulse Rate
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up to 48 hours following drug administration
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Number of subjects with adverse events
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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Number of subjects with clinically significant changes in 12-lead ECG (electrocardiogram)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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Assessment of tolerability by investigator on a 4-point scale
大体时间:after 48 hours following drug administration
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after 48 hours following drug administration
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次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
大体时间:up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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tmax (time from dosing to maximum concentration)
大体时间:up to 48 hours following drug administration
|
up to 48 hours following drug administration
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AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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λz (terminal rate constant in plasma)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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t1/2 (terminal half-life of the analyte in plasma)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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MRT (Mean time of residence of drug molecules in the body after intravascular administration)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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Vz/F (Apparent volume of distribution during the terminal phase after extravascular administration)
大体时间:up to 48 hours following drug administration
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up to 48 hours following drug administration
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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。
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
2004年1月1日
初级完成 (实际的)
2004年9月1日
研究注册日期
首次提交
2014年10月2日
首先提交符合 QC 标准的
2014年10月2日
首次发布 (估计)
2014年10月6日
研究记录更新
最后更新发布 (估计)
2014年10月6日
上次提交的符合 QC 标准的更新
2014年10月2日
最后验证
2014年10月1日
更多信息
与本研究相关的术语
其他研究编号
- 1201.1
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