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临床试验/JPRN-jRCT2031200242
JPRN-jRCT2031200242已完成1 期

A Single-Ascending Dose Study to Investigate the Safety, Tolerability, and Pharmacokinetics of LY3537031 in Healthy Participants - J2S-MC-GZMA

Wakayama Naohiko0 个研究点目标入组 60 人开始时间: 2020年12月15日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 65age old(—)
性别
All

入选标准

  • Are male or female not of childbearing potential
  • - Have a body mass index (BMI) between 19 and 35 kg/m2 and a body weight >= 54kg
  • - Have blood pressure, pulse rate, blood and urine laboratory test results that are acceptable for the study
  • - Have veins suitable for blood sampling

排除标准

  • - Have or used to have health problems or laboratory test results or ECG readings that, in the opinion of the doctor, could make it unsafe to participate, or could interfere with understanding the results of the study
  • - Have a diagnosis or history of cancer or malignant disease within 5 years
  • - Have been treated with prescription and over-the-counter medications that promote weight loss within 3 months prior to screening
  • - Show clinical evidence of syphilis, HIV, hepatitis C, or hepatitis B, and/or test positive
  • - Have undergone any form of bariatric surgery
  • - Have previously completed or withdrawn from this study
  • - Are currently participating in or completed a clinical trial within the last 3 months
  • - Regularly use known drugs of abuse or with positive drug results
  • - Smoke >10 cigarettes per day or the equivalent, or are unable or unwilling to refrain from nicotine during CRU admission

研究者

发起方
Wakayama Naohiko

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