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临床试验/JPRN-jRCT2080222069
JPRN-jRCT2080222069已完成1 期

A Single-Dose and Multiple-Dose, Dose-Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of LY3002813 in Patients with Mild Cognitive Impairment due to Alzheimer's Disease or Mild to Moderate Alzheimer's Disease

Eli Lilly Japan K.K.0 个研究点开始时间: 2013年5月2日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成

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
>= 50age old 至 ot applicable(—)
性别
All

入选标准

  • The study will enroll men or nonfertile women, at least 50 years of age with evidence of memory impairment on the Free and Cued Selective Reminding Test with Immediate Recall (FCSRT-IR), a Mini-Mental State Examination (MMSE) 16 to 30, no history of macrohemorrhage and no more than 4 microhemorrhages on magnetic imaging resonance (MRI), and a positive amyloid scan by florbetapir. Patients with contraindication for MRI, presence of >4 microhemorrhages on MRI, history or evidence on MRI of macrohemorrhage will be excluded.

排除标准

  • 未提供

研究者

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