跳至主要内容
临床试验/NCT07334860
NCT07334860进行中(未招募)1 期

A Two-Period, Open-label, Fixed-Sequence Study to Evaluate the Single-Dose Pharmacokinetics of Two Formulations of MK-1167 in Healthy Participants

Merck Sharp & Dohme LLC1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2026年2月6日最近更新:
干预措施

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
16
试验地点
1
主要终点
Area Under the Curve from Time 0 to Infinity (AUC0-inf) of MK-1167

研究概览

简要总结

Researchers are looking for new ways to treat Alzheimer's disease (AD). AD is a brain disease that causes a gradual decline in memory, thinking, and ability to carry out daily tasks. MK-1167 is a study medicine designed to treat symptoms of AD. Before giving a study medicine to people with a health condition, researchers first do studies in healthy people to find a safe dose of the study medicine.

The goals of the trial are to learn:

  • What happens to different forms of MK-1167 in a healthy person's body over time
  • About the safety of MK-1167 and if people tolerate it

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
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

  • Is in good health
  • Has a body mass index (BMI) ≥18 and ≤ 32 kg/m^2, inclusive

排除标准

  • Has a history of clinically significant endocrine, gastrointestinal, cardiovascular, hematological, hepatic, immunological, renal, respiratory, genitourinary, or major neurological abnormalities or diseases
  • Is a smoker and/or has used nicotine or nicotine-containing products within the past 3 months.

研究组 & 干预措施

Arm 1: MK-1167 Form 2

Experimental

Participants receive MK-1167 Form 2 orally.

干预措施: MK-1167 (Drug)

Arm 2: MK-1167 Form 1

Experimental

Participants receive MK-1167 Form 1 orally.

干预措施: MK-1167 (Drug)

结局指标

主要结局

Area Under the Curve from Time 0 to Infinity (AUC0-inf) of MK-1167

时间窗: At designated time points (up to approximately 21 days)

Blood samples will be collected to determine the AUC0-inf of MK-1167.

Maximum Plasma Concentration (Cmax) of MK-1167

时间窗: At designated time points (up to approximately 21 days)

Blood samples will be collected to determine the Cmax of MK-1167.

Area Under the Curve from Time 0 to Last Measurable Concentration (AUC0-last) of MK-1167

时间窗: At designated time points (up to approximately 21 days)

Blood samples will be collected to determine the AUC0-last of MK-1167.

次要结局

  • Area Under the Curve from Time 0 to 24 hours (AUC0-24) of MK-1167(At designated time points (up to approximately 24 hours))
  • Concentration at 24 hours (C24) of MK-1167(At designated time points (up to approximately 24 hours))
  • Time to Maximum Serum Concentration (Tmax) of MK-1167(At designated time points (up to approximately 21 days))
  • Apparent Terminal Half-life (t1/2) of MK-1167(At designated time points (up to approximately 21 days))
  • Apparent Clearance after Nonintravenous Administration (CL/F) of MK-1167(At designated time points (up to approximately 21 days))
  • Apparent Volume of Distribution during Terminal Phase (Vz/F) of MK-1167(At designated time points (up to approximately 21 days))
  • Number of Participants Who Experience One or More Adverse Events (AEs)(Up to approximately 78 days)
  • Number of Participants Who Discontinue Study Intervention Due to an AE(Up to approximately 36 days)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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