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临床试验/NCT03522129
NCT03522129已完成1 期

A Pilot Study to Evaluate the Effect of CT1812 Treatment on Amyloid Beta Oligomer Displacement Into CSF in Subjects With Mild to Moderate Alzheimer's Disease

Cognition Therapeutics2 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2018年5月30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
入组人数
3
试验地点
2
主要终点
Measuring the displacement of Amyloid beta oligomers into cerebrospinal fluid (CSF)

研究概览

简要总结

This is a multi-center, Phase 1b, randomized, double-blind, placebo-controlled parallel-group trial in adults with mild to moderate AD.

详细描述

This is a multi-center, Phase 1b, randomized, double-blind, placebo-controlled parallel-group trial in adults with mild to moderate AD. The primary endpoint is the change from the baseline CSF Amyloid beta oligomer concentration after dosing with CT1812 versus placebo. The change from baseline will be measured through a number of exploratory endpoints as indicated below. For each subject, the baseline CSF oligomer concentration will be computed as the average of the measurements from hours -4, -3, -2 and -1 and 0.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Double-blind for study site and participants

入排标准

年龄范围
50 Years 至 80 Years(Adult, 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

Active Treatment- CT1812 560 mg

Active Comparator

干预措施: CT1812 (Drug)

Active Treatment- CT1812 280 mg

Active Comparator

干预措施: CT1812 (Drug)

Active Treatment- CT1812 90 mg

Active Comparator

干预措施: CT1812 (Drug)

Placebo Comparator - Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Measuring the displacement of Amyloid beta oligomers into cerebrospinal fluid (CSF)

时间窗: 48 hours

evidence of oligomer displacement as demonstrated by a clear rise in CSF oligomer concentration relative to baseline and placebo

次要结局

未报告次要终点

研究者

发起方
Cognition Therapeutics
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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