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临床试验/NCT01396265
NCT01396265已完成1 期

Relative Bioavailability of a Single Oral Dose of 40 mg Afatinib Given Alone and After Multiple Doses of Rifampicin - an Open-label, Two-period, Fixed Sequence Clinical Phase I Trial in Healthy Male Volunteers

Boehringer Ingelheim1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2011年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
22
试验地点
1
主要终点
Area Under Curve From 0 to Infinity Hours (AUC0-∞)

研究概览

简要总结

The objective of the current study is to investigate the effect of the P-gp inducer rifampicin on the pharmacokinetics (PK) of afatinib in healthy male volunteers

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Rifampicin + Afatinib (Test)

Experimental

Tablet, Oral administration with 240 mL of water

干预措施: Afatinib (Drug)

Afatinib alone (Reference)

Experimental

Tablet, Oral administration with 240 mL of water

干预措施: Afatinib (Drug)

Rifampicin + Afatinib (Test)

Experimental

Tablet, Oral administration with 240 mL of water

干预措施: Rifampicin (Drug)

结局指标

主要结局

Area Under Curve From 0 to Infinity Hours (AUC0-∞)

时间窗: 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose

AUC0-∞ represents the area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity.

Area Under Curve From 0 to tz (AUC0-tz)

时间窗: 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose

AUC0-tz represents the area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable drug plasma concentration.

Maximum Concentration (Cmax)

时间窗: 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose

Cmax represents the maximum concentration of the analyte in plasma.

次要结局

  • Time From Dosing to the Maximum Concentration of Afatinib in Plasma (Tmax)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Terminal Half-life of Afatinib in Plasma (t1/2)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Area Under Curve From 0 to 24 h (AUC0-24)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Percentage of the AUCtz-∞ Obtained by Extrapolation (%AUCtz-∞)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Mean Residence Time of Afatinib in the Body After Oral Administration (MRTpo)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Apparent Clearance of Afatinib in the Plasma After Extravascular Administration (CL/F)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)
  • Apparent Volume of Distribution During the Terminal Phase lambda_z Following an Extravascular Dose (V_z/F)(0.5, 1, 2, 3, 4, 5, 6, 7, 8, 10, 12, 24, 36, 48, 72, 96, 120 hours post dose)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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