Study of Pharmacokinetic Interaction Between Combivir® (ZDV+3TC) and BILR 355 BS Plus Ritonavir in Healthy Subjects
2014年10月2日 更新者:Boehringer Ingelheim
Study of Pharmacokinetic Interaction Between Combivir® (ZDV+3TC) and BILR 355 BS Plus Ritonavir
Study to determine the effect of BILR 355/r on Combivir® pharmacokinetics and the effect of Combivir® on BILR 355 BS pharmacokinetics.
研究概览
研究类型
介入性
注册 (实际的)
51
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 59年 (成人)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Males or females who meet the inclusion/exclusion criteria, females are not pregnant or nursing, and agree to use a double-barrier method of birth control (condoms or diaphragm plus spermicide) throughout the trial (alone or in addition to other methods of birth control such as oral contraceptives)
- Age ≥18 and <60 years
- Body Mass Index (BMI) ≥18.5 and BMI ≤29.9 kg/m2
- Ability to give signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local regulations
Exclusion Criteria:
- Current (symptomatic within the last 30 days) and medically relevant gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Surgery of gastrointestinal tract (except appendectomy)
- Currently active (symptomatic within the last 30 days) diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of relevant orthostatic hypotension, fainting spells or blackouts
- 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 one month prior to administration of study drug or during the trial (review with clinical monitor if questionable)
- Use of drugs within 10 days prior to administration or during the trial, which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation (review with clinical monitor if questionable)
- Participation in another trial with an investigational drug within one month prior to administration or during the trial
- Current smoker
- Alcohol (more than 60 g/day) or drug abuse (positive urine test for illicit prescription or non-prescription drugs or drugs of abuse).
- Recent blood donation (more than 100 mL within 4 weeks prior to administration or during the trial)
- Excessive physical activities (within 1 week prior to study drug administration or during the trial)
- Any laboratory value outside the normal reference range that is of clinical relevance at screening, according to the judgment of the investigator
- Inability to comply with dietary regimen required by the protocol
- Chronic or relevant acute infections
- Infected with hepatitis B or hepatitis C viruses (defined as either being hepatitis B surface antigen, or hepatitis C antibody positive)
- HIV-1 infected as defined by a positive HIV ELISA test
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:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Combivir® plus BILR 355/Ritonavir
|
其他名称:
|
|
实验性的:BILR 355/Ritonavir
|
其他名称:
|
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 plasma over one dosing interval at steady state (AUC0-12h,ss)
大体时间:up to day 18
|
up to day 18
|
|
Maximum measured concentration of the analyte in plasma at steady state over a dosing interval τ (Cmax,ss)
大体时间:up to day 18
|
up to day 18
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Apparent clearance of the analyte in plasma following extravascular administration at steady state (CL/F,ss)
大体时间:up to day 18
|
up to day 18
|
|
Time from dosing to the maximum concentration of the analyte in plasma at steady state (tmax,ss)
大体时间:up to day 18
|
up to day 18
|
|
Terminal half-life of the analyte in plasma at steady state (t1/2,ss)
大体时间:up to day 18
|
up to day 18
|
|
Apparent volume of distribution during the terminal phase λz at steady state following an extravascular dose (Vz/Fss)
大体时间:up to day 18
|
up to day 18
|
|
Measured concentration of the analyte in plasma 12 hours post last dose at steady state (Cp12h, ss)
大体时间:up to day 18
|
up to day 18
|
|
Number of subjects with adverse events
大体时间:up to 49 days
|
up to 49 days
|
|
Number of subjects with abnormal laboratory parameters
大体时间:up to 49 days
|
up to 49 days
|
|
Number of subjects with clinically significant findings in vital signs
大体时间:up to 49 days
|
up to 49 days
|
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10月1日
初级完成 (实际的)
2005年5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
其他相关的 MeSH 术语
其他研究编号
- 1188.9
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.