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临床试验/NCT04135833
NCT04135833已完成1 期

A Phase I Study to Assess the Effect of Itraconazole and Rifampicin on Pharmacokinetics Profile of BPI-7711 in Chinese Healthy Volunteers

Beta Pharma, Inc.1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2019年12月12日最近更新:
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
31
试验地点
1
主要终点
Cmax

研究概览

简要总结

This is a phase I study to assess the effect of itraconazole and rifampicin on the pharmacokinetic parameters of BPI-7711 in Chinese healthy volunteers.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Male, aged from 18 to 45 years
  • BMI from 18.5 to 28.0 kg/m2
  • Medical history, vital signs, physical examination and lab tests are normal or abnormal without clinical significance

排除标准

  • Subjects with clinical significant diseases
  • Subjects with allergic disease history
  • Subjects with gastrointestinal disease history that can affect study drug absorption
  • Subjects with drug abuse history

研究组 & 干预措施

Itraconazole and BPI-7711

Experimental

BPI-7711 alone followed by BPI-7711 +Itraconazole, followed by Itraconazole alone.

干预措施: BPI-7711 (Drug)

Itraconazole and BPI-7711

Experimental

BPI-7711 alone followed by BPI-7711 +Itraconazole, followed by Itraconazole alone.

干预措施: Itraconazole (Drug)

Rifampicin and BPI-7711

Experimental

BPI-7711 alone followed by BPI-7711 +Rifampicin, followed by Rifampicin alone.

干预措施: BPI-7711 (Drug)

Rifampicin and BPI-7711

Experimental

BPI-7711 alone followed by BPI-7711 +Rifampicin, followed by Rifampicin alone.

干预措施: Rifampicin (Drug)

结局指标

主要结局

Cmax

时间窗: Blood samples collected on Day 1 and Day 20 (arm 1)/Day 25 (arm 2) at pre-dose, 1, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72, 96, 120, 144, 168 and 336 hours post BPI-7711 dose

Pharmacokinetics of BPI-7711 by assessment of maximum plasma concentration

AUC(0-last)

时间窗: Blood samples collected on Day 1 and Day 20 (arm 1)/Day 25 (arm 2) at pre-dose, 1, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72, 96, 120, 144, 168 and 336 hours post BPI-7711 dose

Pharmacokinetics of BPI-7711 by assessment of area under the plasma concentration time curve from zero to last assessed timepoint

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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