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临床试验/NCT03979248
NCT03979248已完成1 期

An Open-Label, Single-Sequence Study to Investigate the Effects of Gastric Acid Suppression by Rabeprazole on the Pharmacokinetics of BMS-986165 in Healthy Participants

Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2019年5月16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
入组人数
21
试验地点
1
主要终点
Area Under the Plasma Concentration-time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC[0-T]) of BMS-986165

研究概览

简要总结

The purpose of this study is to evaluate the effects of stomach acid suppression by rabeprazole and BMS-986165 on how fast and complete the drug is absorbed into the body of healthy participants.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Any major surgery within 4 weeks of study drug administration
  • Use of any prescription drugs or over-the-counter acid controllers
  • Positive urine screen for drugs of abuse, alcohol, or cotinine
  • History of allergy to BMS-986165, rabeprazole, or related compounds
  • Other protocol inclusion/exclusion criteria may apply.

研究组 & 干预措施

BMS-986165 + Rabeprazole

Experimental

干预措施: BMS-986165 (Drug)

BMS-986165 + Rabeprazole

Experimental

干预措施: Rabeprazole (Drug)

结局指标

主要结局

Area Under the Plasma Concentration-time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUC[0-T]) of BMS-986165

时间窗: Day 1 and Day 9

Area Under the Plasma Concentration-time Curve From Time Zero Extrapolated to Infinite Time (AUC[INF]) of BMS-986165

时间窗: Day 1 and Day 9

Maximum Observed Plasma Concentration (Cmax) of BMS-986165

时间窗: Day 1 and Day 9

次要结局

  • Percentage of Participants with Clinical Laboratory Values, Vital Signs, and Electrocardiograms (ECGs)(Up to Day 12)
  • Percentage of Participants with Adverse Events (AEs)(Up to Day 12)

研究者

发起方
Bristol-Myers Squibb
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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