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Relative Oral Bioavailability of BI 44847 as Suspension Compared to Tablet and the Influence of Food Anf of BI 44847 as Solution Compared to Tablet in Healthy Male Volunteers

2014年8月7日 更新者:Boehringer Ingelheim

Relative Oral Bioavailability of 400 mg BI 44847 as Suspension Compared to 400 mg BI 44847 as Tablet and the Influence of Food (Standardised High Fat Breakfast) on the Tablet in a Single Dose, Open-label, Randomised Three-way Crossover Trial and Relative Oral Bioavailability of 40 mg BI 44847 as Solution Compared to 40 mg BI 44847 as Tablet in Healthy Male Volunteers in a Single Dose, Open-label, Randomised Two-way Crossover Trial

Study to investigate the relative oral bioavailability of 400 mg BI 44847 as suspension vs. 400 mg BI 44847 as tablet, to investigate a food effect on the 400 mg tablet pharmacokinetic (PK) and to investigate relative oral bioavailability of 40 mg BI 44847 as solution vs. 40 mg BI 44847 as tablet.

研究概览

研究类型

介入性

注册 (实际的)

25

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

21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
  • Age ≥ 21 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 and the local legislation

Exclusion Criteria:

  • Any finding of the medical examination (including BP, PR and ECG) deviating from normal and of clinical relevance
  • Any evidence of a clinically relevant concomitant disease
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  • History of relevant orthostatic hypotension, fainting spells or blackouts
  • Chronic or relevant acute infections
  • History of relevant allergy/hypersensitivity (including allergy to drug or its excipients)
  • Intake of drugs with a long half-life (> 24 hours) within at least one month or less than 10 half-lives of the respective drug prior to administration or during the trial
  • Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to administration or during the trial
  • Participation in another trial with an investigational drug within two months prior to administration or during the trial
  • Smoker (> 10 cigarettes or > 3 cigars or > 3 pipes/day)
  • Inability to refrain from smoking on trial days
  • Alcohol abuse (more than 60 g/day)
  • Drug abuse
  • Blood donation (more than 100 mL) within four weeks prior to administration or during the trial
  • Excessive physical activities (within one week prior to administration or during the trial)
  • Any laboratory value outside the reference range that is of clinical relevance
  • Inability to comply with dietary regimen of study centre
  • Any ECG value outside of the reference range and of clinical relevance including, but not limited to QRS interval > 120 ms. A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval > 450 ms or QT> 500 ms)
  • A history of additional risk factors for torsade de pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
  • The use of concomitant medications that prolong the QT/QTc interval

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:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Treatment A
BI 44847 suspension high dose, fasted
实验性的:Treatment B
BI 44847 tablet high dose, fasted
实验性的:Treatment C
BI 44847 tablet high dose, fed
有源比较器:Treatment D
BI 44847 solution low dose, fasted
实验性的:Treatment E
BI 44847 tablet low dose, fasted

研究衡量的是什么?

主要结果指标

结果测量
大体时间
AUC0-∞(血浆中分析物在从 0 外推到无穷大的时间间隔内的浓度-时间曲线下面积)
大体时间:给药后最多 48 小时
给药后最多 48 小时
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of the last quantifiable data point)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Cmax (maximum concentration of the analyte in plasma)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration

次要结果测量

结果测量
大体时间
研究者根据 4 分制评估耐受性
大体时间:第 3 天
第 3 天
λz(血浆中的终末速率常数)
大体时间:给药后最多 48 小时
给药后最多 48 小时
t1/2(分析物在血浆中的终末半衰期)
大体时间:给药后最多 48 小时
给药后最多 48 小时
Vz/F(血管外给药后终末期 λz 的表观分布容积)
大体时间:给药后最多 48 小时
给药后最多 48 小时
fet1-t2(从时间点 t1 到时间点 t2 尿液中消除的分析物的分数)
大体时间:给药后最多 48 小时
给药后最多 48 小时
CLR,t1-t2(分析物从时间点 t1 到时间点 t2 的肾脏清除率)
大体时间:给药后最多 48 小时
给药后最多 48 小时
%AUCtz-∞(外推得到的AUC0-∞的百分比)
大体时间:给药后最多 48 小时
给药后最多 48 小时
tmax (time from dosing to maximum concentration)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
MRTpo (mean residence time of the analyte in the body after po administration)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
CL/F (total clearance of the analyte in the plasma after extravascular administration)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Aet1-t2 (amount of analyte that is eliminated in urine from the time point t1 to time point t2)
大体时间:up to 48 hours after drug administration
up to 48 hours after drug administration
Number of patients with clinically relevant changes in vital signs
大体时间:up to 3 days after last drug administration
up to 3 days after last drug administration
Number of patients with clinically relevant findings in 12-lead electrocardiogram (ECG)
大体时间:up to 3 days after last drug administration
up to 3 days after last drug administration
Number of patients with adverse events
大体时间:up to 3 days after last drug administration
up to 3 days after last drug administration

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

2007年1月1日

初级完成 (实际的)

2007年3月1日

研究注册日期

首次提交

2014年8月7日

首先提交符合 QC 标准的

2014年8月7日

首次发布 (估计)

2014年8月8日

研究记录更新

最后更新发布 (估计)

2014年8月8日

上次提交的符合 QC 标准的更新

2014年8月7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

  • 1224.2

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.

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