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Influence of Food on the Bioavailability of Two Doses of Telmisartan/HCTZ Fixed-dose Combination in Japanese Healthy Male Volunteers

2014年10月27日 更新者:Boehringer Ingelheim

Influence of Food on the Bioavailability of Telmisartan 40 mg/HCTZ 12.5 mg Fixed-dose Combination and of Telmisartan 80 mg/HCTZ 12.5 mg Fixed-dose Combination in Japanese Healthy Male Volunteers (an Open-label, Randomised, Single-dose, Two-way Crossover Study)

To investigate the relative bioavailability and pharmacokinetics of the fixed-dose combination tablets (telmisartan 40 mg/HCTZ 12.5 mg and telmisartan 80 mg/HCTZ 12.5 mg) after food intake in comparison with those in the fasting state in healthy Japanese male volunteers

研究概览

研究类型

介入性

注册 (实际的)

32

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

20年 至 35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:

  1. Based upon a complete medical history, including the physical examination, vital signs (blood pressure (BP), pulse rate (PR), body temperature), 12-lead ECG (electrocardiogram), clinical laboratory tests
  2. Age ≥20 and Age ≤35 years
  3. Body weight ≥50 kg
  4. BMI ≥18.0 and BMI ≤25.0 kg/m2 (Body Mass Index)
  5. 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:

  1. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  2. Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  3. Chronic or relevant acute infections
  4. Any clinical relevant findings of the laboratory test deviating from normal
  5. Positive result for either hepatitis B surface (HBs) antigen, anti Hepatitis C virus (HCV) antibodies, syphilitic test or human immunodeficiency virus (HIV) test
  6. History of surgery of gastrointestinal tract (except appendectomy)
  7. History of relevant orthostatic hypotension, fainting spells or blackouts
  8. Known hypersensitivity to any component of the formulation (telmisartan and hydrochlorothiazide), or to any other angiotensin II receptor blocker (ARBs), any other thiazides, or thiazide derivatives (e.c. sulfonamide derivatives like a chlorthalidone)
  9. 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
  10. Use of drugs which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 7 days prior to administration or during the trial
  11. Participation in another trial with an investigational drug within 4 months or 6 half-lives of the investigational drug prior to administration
  12. Smoker (≥20 cigarettes/day)
  13. Alcohol abuse (60 g or more ethanol/day: ex. 3 middle-sized bottles of beer, 3 gous (equivalent to 540 mL) of sake)
  14. Drug abuse
  15. Blood donation (more than 100 mL within 4 weeks prior to administration or during the trial)
  16. Excessive physical activities (within 1 week prior to administration or during the trial)
  17. Intake of alcohol within 2 days prior to administration
  18. Inability to comply with dietary regimen of study centre
  19. Inability to refrain from smoking on trial days
  20. Subjects judged to be inappropriate by the investigator or the sub-investigator

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
实验性的:Telmisartan low / HCTZ fixed-dose combination, fed
实验性的:Telmisartan high / HCTZ fixed-dose combination, fed
有源比较器:Telmisartan low /HCTZ fixed-dose combination, fasted
有源比较器:Telmisartan high /HCTZ fixed-dose combination, fasted

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Area under the concentration-time curve of the analyte in the plasma over the time interval from 0 to the time of the last quantifiable data point (AUC0-tz)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
The maximum measured concentration of the analyte in the plasma (Cmax)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration

次要结果测量

结果测量
大体时间
在生命体征方面有临床意义发现的参与者人数
大体时间:最后一次给药后最多 72 小时
最后一次给药后最多 72 小时
口服给药后分析物在体内的平均停留时间(MRTpo)
大体时间:给药后最多 72 小时
给药后最多 72 小时
Area under the concentration-time curve of the analyte in the plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Time from dosing to the maximum concentration of the analyte in the plasma (tmax)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Terminal rate constant in the plasma (λz)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Terminal half-life of the analyte in the plasma (t1/2)
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Number of participants with abnormal findings in physical examination
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Number of participants with clinically significant findings in 12-lead ECG
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Number of participants with clinically significant findings in clinical laboratory parameters
大体时间:Up to 72 hours after drug administration
Up to 72 hours after drug administration
Number of participants with adverse events
大体时间:Up to 7 days after drug administration
Up to 7 days after 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

2008年7月1日

初级完成 (实际的)

2008年8月1日

研究注册日期

首次提交

2014年10月27日

首先提交符合 QC 标准的

2014年10月27日

首次发布 (估计)

2014年10月28日

研究记录更新

最后更新发布 (估计)

2014年10月28日

上次提交的符合 QC 标准的更新

2014年10月27日

最后验证

2014年10月1日

更多信息

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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