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A Study To Assess The Anidulafungin And Voriconazole Concentration In Lung Following Intravenous Administration In Healthy Subjects

2010年1月5日 更新者:Pfizer

A Phase 4, Open Label Study To Assess The Bronchopulmonary Pharmacokinetics Of Anidulafungin And Voriconazole Following Intravenous Administration In Healthy Subjects

The purpose of this study is to provide anidulafungin and voriconazole to healthy subjects to determine the drug concentration in the lung.

研究概览

研究类型

介入性

注册 (实际的)

24

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Connecticut
      • Hartford、Connecticut、美国、06102
        • Pfizer Investigational Site

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 55年 (成人)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Healthy adult subjects willing to comply with the study requirement.

Exclusion Criteria:

  • Clinical significant disease.
  • Sensitive to study medication.
  • Not willing to comply with the study requirement.

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

  • 分配:随机化
  • 介入模型:单组作业
  • 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:1个
Subjects will be admitted to the clinical research unit on Day 0. Subjects will receive anidulafungin intravenously in a loading dose of 200 mg on Day 1, followed by maintenance doses of 100 mg Q24h on Day 2 and Day 3. Simultaneously, using a separate intravenous access, subjects will receive voriconazole in a loading dose of 6 mg/kg Q12h on Day 1, followed by a maintenance dose of 4 mg/kg Q12h on Day 2, and a 4 mg/kg morning dose on Day 3.

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
Plasma Pharmacokinetics (PK): Maximum Observed Plasma Concentration (Cmax)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Cmax = maximum observed plasma concentration; measured in micrograms per milliliter (ug/mL). Observed directly from the data. Collected on Day 3.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Plasma PK: Time to Reach Maximum Plasma Concentration (Tmax)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Tmax = time (hours) to maximum plasma concentration (Cmax). Observed directly from data as time of first occurrence. Collected on Day 3.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Plasma PK: Area Under the Curve From Time Zero to Time = Tau (AUCtau)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
AUCtau = area under the plasma concentration-time profile from time zero (0) to time = t (AUCt), the dosing interval, where t is 24 hours for anidulafungin and 12 hours for voriconazole; measured as micrograms times hours per milliliter (ug*hr/mL). Collected on Day 3.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Plasma PK: Plasma Elimination Half-life (t1/2)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
t1/2 = terminal elimination half-life in hours; Loge(2)/Kel, where Kel is the terminal phase rate constant calculated by a linear regression of the log-linear concentration-time curve. Collected on Day 3.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Plasma PK: Total Clearance (CL Total)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
CL total = total clearance calculated as dose divided by AUCt; measured as milliliters per minute (mL/min). Collected on Day 3.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Plasma PK: Volume of Distribution at Steady-state (Vss)
大体时间:100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Vss = volume of distribution at steady-state; measured as liters (L). Calculated as (CL multiplied by mean residence time extrapolated to infinity [MRTinf]). MRTinf = [(AUMCt plus t (AUCinf minus AUCt)) divided by AUCt] minus (infusion time divided by 2); AUMCt = area under the first moment curve from time zero to time t; AUCinf = area under the plasma concentration-time curve extrapolated to infinity.
100 minutes (end of infusion), 2, 4, 8, 12, 24 hours after start of infusion
Epithelial Lining Fluid (ELF) PK: Cmax
大体时间:4, 8, 12, 24 hours after start of infusion
Cmax=maximum observed plasma concentration. ELF collected by bronchoscopy and bronchoalveolar lavage (BAL) Day 3; determined from BAL sample using urea dilution method: [Drug ELF]=[Drug BAL] multiplied by [Urea SERUM] divided by [Urea BAL]. Drug ELF=anidulafungin or voriconazole (drug) concentration in ELF corrected for dilution; Drug BAL=assayed drug concentration in BAL; Urea SERUM and Urea BAL simultaneously collected. Summary parameters derived using average data for all subjects; associated to a single subject for reporting purposes (mean with standard deviation not calculated).
4, 8, 12, 24 hours after start of infusion
ELF PK: Tmax
大体时间:4, 8, 12, 24 hours after start of infusion
Tmax = time (hours) to maximum plasma concentration (Cmax). Observed directly from data as time of first occurrence. ELF collected by bronchoscopy and BAL on Day 3.
4, 8, 12, 24 hours after start of infusion
ELF PK: AUCtau
大体时间:4, 8, 12, 24 hours after start of infusion
AUCtau = area under the plasma concentration-time profile from time zero (0) to time = t (AUCt), the dosing interval, where t is 24 hours for anidulafungin and 12 hours for voriconazole. ELF collected by bronchoscopy and BAL on Day 3. Summary parameters were derived using average data for all subjects and associated to a single subject for reporting purposes (mean with standard deviation was not calculated).
4, 8, 12, 24 hours after start of infusion
ELF PK: t1/2
大体时间:4, 8, 12, 24 hours after start of infusion
t1/2 = terminal elimination half-life in hours; Loge(2)/Kel, where Kel is the terminal phase rate constant calculated by a linear regression of the log-linear concentration-time curve. ELF collected by bronchoscopy and BAL on Day 3.
4, 8, 12, 24 hours after start of infusion
Alveolar Macrophages (AM): Cmax
大体时间:4, 8, 12, 24 hours after start of infusion
Cmax = maximum observed plasma concentration; observed directly from the data. AM collected by bronchoscopy and BAL on Day 3. Summary parameters were derived using average data for all subjects and associated to a single subject for reporting purposes (mean with standard deviation was not calculated).
4, 8, 12, 24 hours after start of infusion
AM: Tmax
大体时间:4, 8, 12, 24 hours after start of infusion
Tmax = time (hours) to maximum plasma concentration (Cmax). Observed directly from data as time of first occurrence. AM collected by bronchoscopy and BAL on Day 3.
4, 8, 12, 24 hours after start of infusion
AM: AUCtau
大体时间:4, 8, 12, 24 hours after start of infusion
AUCtau = area under the plasma concentration-time profile from time zero (0) to time = t (AUCt), the dosing interval, where t is 24 hours for anidulafungin and 12 hours for voriconazole. AM collected by bronchoscopy and BAL on Day 3. Summary parameters were derived using average data for all subjects and associated to a single subject for reporting purposes (mean with standard deviation was not calculated).
4, 8, 12, 24 hours after start of infusion
AM: t1/2
大体时间:4, 8, 12, 24 hours after start of infusion
t1/2 = terminal elimination half-life in hours; Loge(2)Kel, where Kel is the terminal phase rate constant calculated by a linear regression of the log-linear concentration-time curve. AM collected by bronchoscopy and BAL on Day 3.
4, 8, 12, 24 hours after start of infusion
Overall Drug Penetration Ratio in ELF
大体时间:4, 8, 12, 24 hours after start of infusion
ELF collected by bronchoscopy and BAL on Day 3. ELF to plasma penetration ratio calculated by dividing area under the plasma concentration-time profile (AUC) in ELF by AUC in plasma from 20 subjects where t is 24 hours for anidulafungin and 12 hours for voriconazole. Summary parameters were derived using average data for all subjects and associated to a single subject for reporting purposes (mean with standard deviation was not calculated).
4, 8, 12, 24 hours after start of infusion
Concentration Ratio in ELF to Plasma
大体时间:4, 8, 12, 24 hours after start of infusion
Concentration ratio in ELF to plasma determined by a point estimate within each subject at the time-point where ELF data was available.
4, 8, 12, 24 hours after start of infusion

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。

赞助

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。

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9月1日

初级完成 (实际的)

2008年10月1日

研究完成 (实际的)

2008年10月1日

研究注册日期

首次提交

2009年7月13日

首先提交符合 QC 标准的

2009年7月14日

首次发布 (估计)

2009年7月15日

研究记录更新

最后更新发布 (估计)

2010年2月9日

上次提交的符合 QC 标准的更新

2010年1月5日

最后验证

2010年1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.

anidulafungin and voriconazole的临床试验

3
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