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临床试验/JPRN-jRCT2080223944
JPRN-jRCT2080223944已完成2 期

Assessment of Safety, Tolerability, and Efficacy of LY3303560 in Early Symptomatic Alzheimer's Disease (I8G-MC-LMDC)

Eli Lilly Japan K.K.0 个研究点目标入组 360 人开始时间: 2018年6月14日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
360

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
>= 60age old 至 <= 85age old(—)
性别
All

入选标准

  • Participants must have gradual and progressive change in memory function for >6 months.
  • - Participants must have a family member or close friend who is with you at least 10 hours per week and can attend study appointments.

排除标准

  • - Participants must not have significant neurological disease affecting the nervous system, other than AD, that affects cognition or may affect completion of the study.
  • - Participants must not have serious or unstable illness that could interfere with the analysis of the study or has a life expectancy <24 months.
  • - Participants must not have history of cancer within the last 5 years with the exception of certain types of skin, cervical, prostate, and other cancers that are not likely to recur or spread.
  • - Participants must not have serious risk for suicide.
  • - Participants must not have history of drug or alcohol use disorder within the last 2 years.
  • - Participants must not have multiple severe drug allergies
  • - Participants must not have HIV, Hepatitis B or Hepatitis C
  • - Participants must not be receiving gamma globulin (IgG) or intravenous immunoglobulin (IVIG) therapy

研究者

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