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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide in Healthy Male Volunteers

2014年10月7日 更新者:Boehringer Ingelheim

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2 μg/5 μg, 10 μg/5 μg, and 40 μg/10 μg) of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide for 14 Days in Healthy Male Volunteers (Double-blind, Randomised, Placebo Controlled [at Each Dose Level] Study)

To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL and Tiotropium Bromide when given as fixed dose combination

研究概览

研究类型

介入性

注册 (实际的)

36

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 45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 male based upon a complete medical history, including physical examination, regarding vital signs (BP, PR), 12-lead ECG measurement, and clinical laboratory tests. There is no finding deviating from normal and of clinical relevance. There is no evidence of a clinically relevant concomitant disease
  • Age ≥21 and ≤45 years
  • BMI ≥18.5 and <30 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 BP, PR, and ECG measurements) deviating from normal and of clinical relevance
  • 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 the drug or its excipients) as judged clinically relevant by the investigator
  • Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomization
  • 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 randomisation
  • Participation in another trial with an investigational drug within 2 months prior to randomisation
  • Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
  • Inability to refrain from smoking on trial days as judged by the investigator
  • Alcohol abuse (more than 40 g alcohol a day)
  • Drug abuse
  • Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)
  • Excessive physical activities within 1 week prior to randomisation or during the trial
  • Any laboratory value outside the reference range that is of clinical relevance
  • Inability to comply with dietary regimen of the study centre

The following exclusion criteria are specific for this study due to the known class side effect profile of ß2-mimetics:

  • Asthma or history of pulmonary hyperreactivity
  • Hyperthyrosis
  • Allergic rhinitis in need of treatment
  • Clinically relevant cardiac arrhythmia
  • Paroxysmal tachycardia (>100 beats per minute)

The following exclusion criteria are specific for this study due to the known class side effect profile of Tiotropium:

  • Hypersensitivity to tiotropium and/or related drugs of these classes
  • History of narrow-angle glaucoma
  • History of prostatic hyperplasia
  • History of bladder-neck obstruction

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:BI 1744 CL in combination with Tiotropium

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 clinically relevant findings in physical examination
大体时间:Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in vital signs
大体时间:Up to day 32
blood pressure, pulse rate
Up to day 32
Number of subjects with clinically relevant findings in 12-lead ECG
大体时间:Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in laboratory tests
大体时间:Up to day 32
Up to day 32
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
大体时间:up to 318 hours after start of treatment
Systemic metabolic parameters: cyclic adenosine mono phosphate (cAMP) and potassium
up to 318 hours after start of treatment
Number of subjects with clinically relevant changes in airway resistance (Raw) measured by body plethysmography
大体时间:Pre-dose, up to 408 hours after start of treatment
Pre-dose, up to 408 hours after start of treatment
Number of subjects with adverse events
大体时间:Up to day 32
Up to day 32
Global assessment of tolerability by investigator on a 4-point scale
大体时间:Up to day 32
Up to day 32

次要结果测量

结果测量
大体时间
Maximum concentration in plasma (Cmax)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Time from dosing to maximum concentration in plasma (tmax)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Area under the concentration-time curve in plasma (AUC)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Area under the concentration-time curve in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Percentage of AUC 0-∞ that is obtained by extrapolation (%AUCtz-∞)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Terminal rate constant in plasma (λz)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Terminal half-life in plasma (t½)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Mean residence time in the body after inhalation (MRTih)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Apparent clearance after extravascular administration (CL/F)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Apparent volume of distribution during the terminal phase λz following an extravascular dose (Vz/F)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Amount eliminated in urine from the time point t1 to t2 (Aet1-t2)
大体时间:up to 336 hours after start of treatment
up to 336 hours after start of treatment
Fraction excreted in urine from time point t1 to t2 (fet1-t2)
大体时间:up to 336 hours after start of treatment
up to 336 hours after start of treatment
Renal clearance from the time point t1 until the time point t2 (CLR,t1-t2)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Minimum measured concentration in plasma at steady state over a uniform dosing interval τ (Cmin,ss)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Predose concentration of the analytes in plasma at steady state immediately before administration of the next dose (Cpre,ss)
大体时间:Pre-dose every 24 hours
Pre-dose every 24 hours
Time of last measurable concentration in plasma (tz)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Linearity index (LI)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Accumulation ratio based on Cmax (RA,Cmax)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment
Accumulation ratio based on AUCτ (RA,AUC)
大体时间:up to 504 hours after start of treatment
up to 504 hours after start of treatment

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4月1日

初级完成 (实际的)

2007年9月1日

研究注册日期

首次提交

2014年10月7日

首先提交符合 QC 标准的

2014年10月7日

首次发布 (估计)

2014年10月9日

研究记录更新

最后更新发布 (估计)

2014年10月9日

上次提交的符合 QC 标准的更新

2014年10月7日

最后验证

2014年10月1日

更多信息

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