JPRN-jRCT2080223944已完成2 期
Assessment of Safety, Tolerability, and Efficacy of LY3303560 in Early Symptomatic Alzheimer's Disease (I8G-MC-LMDC)
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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