跳至主要内容
临床试验/NL-OMON38581
NL-OMON38581已完成不适用

A STUDY OF THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF LY3045697 AFTER MULTIPLE ORAL DOSING IN HEALTHY SUBJECTS - ASEB

Chorus, Eli Lilly and company0 个研究点目标入组 24 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
24

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
18 至 99(—)

入选标准

  • -Healthy males or females (females must be postmenopausal or surgically sterile)
  • -Postmenopausal female subjects must be between the ages of 45 and 65 years, inclusive
  • -Male subjects and surgically sterile females must be between the ages of 18 and 65 years, inclusive
  • -BMI between 18.0 and 32.5 kg/m2 , inclusive

排除标准

  • Suffering from hepatitis B, hepatitis C, cancer or HIV/AIDS. In case of participation in another drug study within 60days before the start of this study or being a blood donor within 60 days from the start of the study. In case ofdonating more than 1.5 liters of blood in the 10 months prior the start of this study.

研究者

发起方
Chorus, Eli Lilly and company

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