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临床试验/NCT05577624
NCT05577624已完成1 期

An Open-label Study to Evaluate the Drug-drug Interaction Effect of Rifampin, a CYP3A4 Inducer, on the Pharmacokinetics of AMG 510 in Healthy Subjects

Amgen1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2019年11月5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
发起方
Amgen
入组人数
14
试验地点
1
主要终点
Area Under the Plasma Concentration-time Curve (AUC) from Time Zero to Time of Last Quantifiable Concentration (AUClast) of AMG 510

研究概览

简要总结

The primary objective of this study is to evaluate the pharmacokinetic (PK) profile of AMG 510 alone and in combination with rifampin in healthy participants.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy male participants or female participants, between 18 and 60 years of age (inclusive), at the time of Screening.
  • Body mass index, between 18 and 30 kg/m2 (inclusive), at the time of Screening.
  • Females of nonchildbearing potential

排除标准

  • Inability to swallow oral medication or history of malabsorption syndrome.
  • History of hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, unless approved by the Investigator (or designee) and in consultation with the Sponsor.
  • Poor peripheral venous access.
  • History or evidence, at Screening or Check in, of clinically significant disorder, condition, or disease not otherwise excluded that, in the opinion of the Investigator (or designee), would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.

研究组 & 干预措施

AMG 510 + Rifampin

Experimental

干预措施: AMG 510 (Drug)

AMG 510 + Rifampin

Experimental

干预措施: Rifampin (Drug)

结局指标

主要结局

Area Under the Plasma Concentration-time Curve (AUC) from Time Zero to Time of Last Quantifiable Concentration (AUClast) of AMG 510

时间窗: Days 1, 3 and 8

AUC from Time Zero to Infinity (AUCinf) of AMG 510

时间窗: Days 1, 3 and 8

Maximum Plasma Concentration (Cmax) of AMG 510

时间窗: Days 1, 3 and 8

次要结局

  • AUCinf of AMG 510 Metabolite M24(Days 1, 3 and 8)
  • AUClast of AMG 510 Metabolite M24(Days 1, 3 and 8)
  • Cmax of AMG 510 Metabolite M24(Days 1, 3 and 8)
  • Number of Participants with an Adverse Event (AE)(Day 1 to Day 20)

研究者

发起方
Amgen
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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