Pharmacokinetic Properties of Two Dosages Nevirapine Extended Release (XR) Formulations Compared to VIRAMUNE® Tablet as Well as to Nevirapine XR Tablet in Healthy Male Volunteers
2014年7月11日 更新者:Boehringer Ingelheim
An Open-label, Non-randomised, Single-dose, Parallel-group Study of Pharmacokinetic Properties of 200 mg (2 x 100 mg Tablets Once Daily) and 300 mg (3 x 100 mg Tablets Once Daily) Nevirapine Extended Release Formulations Compared to 200 mg VIRAMUNE® Tablet as Well as to 400 mg Nevirapine Extended Release Tablet Following Oral Administration in Healthy Male Volunteers
Study to determine the pharmacokinetic properties of 200 mg (2 x 100 mg tablets once daily) and 300 mg (3 x 100 mg tablets once daily) Nevirapine extended release formulations and to estimate relative bioavailability of these formulations as compared to 200 mg VIRAMUNE® tablet as well as to 400 mg Nevirapine extended release tablet
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
96
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 60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; values within normal ranges or deviating from normal without clinical relevance as considered by the investigator
- Values of Liver Function Test (LFT) have to be within normal ranges
- Age ≥18 and Age ≤60 years
- Body Mass Index (BMI) ≥18.5 and BMI ≤29.9 kg/m2
- Subjects must agree to minimize the risk of female partners becoming pregnant from the first dosing day until 3 months after the completion of the post study medical examination. Acceptable methods of contraception comprises barrier contraception and a medically accepted contraceptive method for the female partner (intra-uterine device with spermicide, hormonal contraceptive since at least two month)
- 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) 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 of clinical relevance
- Surgery of the gastrointestinal tract (except appendectomy and herniotomy)
- 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
- Participation to trial BI 1100.1485 or any other intake of Nevirapine
- 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 trial site
- A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms)
- A history of additional risk factors for Torsades des Pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
- History of disease which affects the present situation
- Inability to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study
- Unlikely to comply with the protocol requirements, instructions and study-related restrictions; e.g., uncooperative attitude, inability to return for follow-up visits, and improbability of completing the study
- Subject is the investigator or any sub-investigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the study
- Vulnerable subjects (e.g. persons kept in detention)
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:非随机化
- 介入模型:并行分配
- 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:Nevirapine XR low dose
|
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实验性的:Nevirapine XR medium dose
|
|
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有源比较器:Nevirapine XR high dose
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有源比较器:Nevirapine (VIRAMUNE®)
commercial product
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
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 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
Cmax (maximum measured concentration of the analyte in plasma)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
次要结果测量
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 36 天
|
最多 36 天
|
|
λz(血浆中的终末速率常数)
大体时间:给药后最多 144 小时
|
给药后最多 144 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 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
tmax (time from dosing to the maximum concentration of the analyte in plasma)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
t1/2 (terminal half-life of the analyte in plasma)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
MRTpo (mean residence time of the analyte in the body after po administration)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
Vz/F (apparent volume of distribution during the terminal phase λz following an extravascular dose)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
ka (absorption rate constant)
大体时间:up to 144 hours after drug administration
|
up to 144 hours after drug administration
|
|
Number of patients with abnormal changes in laboratory parameters
大体时间:Screening, Day 1, 2, 3, 4, 5, 7, 15
|
Screening, Day 1, 2, 3, 4, 5, 7, 15
|
|
Number of patients with clinically significant changes in vital signs (blood pressure (BP), pulse rate (PR))
大体时间:Screening, Day 1, 2, 15
|
Screening, Day 1, 2, 15
|
|
Number of patients with clinically significant changes in 12-lead electrocardiogram (ECG)
大体时间:Screening, Day 1, 15
|
Screening, Day 1, 15
|
|
Assessment of tolerability by investigator on a 4-point scale
大体时间:up to 15 days after drug administration
|
up to 15 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4月1日
初级完成 (实际的)
2008年7月1日
研究注册日期
首次提交
2014年7月8日
首先提交符合 QC 标准的
2014年7月8日
首次发布 (估计)
2014年7月9日
研究记录更新
最后更新发布 (估计)
2014年7月14日
上次提交的符合 QC 标准的更新
2014年7月11日
最后验证
2014年7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.