跳至主要内容
临床试验/NCT05164536
NCT05164536已完成1 期

Plasma P-tau2017 and Quantitative Amyloid PET Imaging in a Cognitively Normal Population

Invicro1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2021年8月27日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Invicro
入组人数
140
试验地点
1
主要终点
Creation of a database of brain amyloid deposition by region using PET signal-to-noise ratio, SUVr .

研究概览

简要总结

The overall goal of this protocol is to compare amyloid burden assessed by amyloid PET to plasma P-tau217 levels.

详细描述

The overall goal of this protocol is to compare amyloid burden assessed by amyloid PET to plasma P-tau217 levels. Other relevant AD-related investigational biomarkers may also be assessed in the provided samples. Apolipoprotein E (ApoE) genetic status will be evaluated with a serum sample.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
70 Years 至 —(Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

[18F]Florbetapir

Experimental

Participants will undergo amyloid PET imaging with an approved amyloid radiotracer (ie, [18F]Florbetapir (Amyvid™)) to assess β-amyloid neuritic plaque density.

干预措施: Amyvid (Drug)

结局指标

主要结局

Creation of a database of brain amyloid deposition by region using PET signal-to-noise ratio, SUVr .

时间窗: 1 year

Amyloid PET imaging will be used to measure regional brain amyloid deposition in each subject.

次要结局

  • Creation of a database of blood P-tau217 and other blood biomarkers.(1 year)

研究者

发起方
Invicro
申办方类型
Other
责任方
Sponsor

研究点 (1)

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