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临床试验/jRCT2080223538
jRCT2080223538已完成3 期

A Phase III,Multicenter,Randomized,Double-Blind,Placebo-Controlled,Parallel-Group,Efficacy And Safety Study of Crenezumab in Patients With Prodromal to Mild Alzheimer's Disease

CHUGAI PHARMACEUTICAL CO.,LTD.1 个研究点目标入组 750 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
750
试验地点
1
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
干预模型
Multicenter,randomized,double-blind,placebo-controlled,parallel-group
主要目的
Treatment Purpose

入排标准

年龄范围
50age old over 至 85age old under(—)
性别
All

入选标准

  • Meet NIA-AA core clinical criteria for probable AD dementia or prodromal AD
  • Having mild symptomatology,as defined by a screening MMSE score of 22 points and higher,and CDR-GS of 0.5 or 1.0

排除标准

  • Any evidence of a condition other than AD that may affect cognition
  • Meet the exclusion criteria of MRI at screening

结局指标

主要结局

-

safety efficacy Observation/Examination

次要结局

未报告次要终点

研究者

研究点 (1)

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