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临床试验/NCT04693520
NCT04693520已完成2 期

A Phase 2, Single-arm Study of the Biomarker Effects of ALZ-801 in Subjects With Early Alzheimer's Disease Who Are Carriers of the ε4 Variant of the Apolipoprotein E Gene (APOE4/4 or APOE3/4)

Alzheon Inc.4 个研究点 分布在 2 个国家目标入组 84 人开始时间: 2020年9月30日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Alzheon Inc.
入组人数
84
试验地点
4
主要终点
Plasma Biomarker of Core AD Pathology

研究概览

简要总结

The study will investigate the effects of oral ALZ-801, in subjects with Early AD who have the APOE4/4 or APOE3/4 genotype, on the biomarkers of core AD pathology. The objectives of this study include determining the efficacy and safety/tolerability of ALZ-801. In addition, the study will evaluate the extended PK profile over 8 hours in 16 subjects after 65 weeks of treatment.

详细描述

The LTE year 1 & 2 study will investigate the effects of oral ALZ-801, in subjects with Early AD who have the APOE4/4 or APOE3/4 genotype, on the biomarkers of core AD pathology. The objectives of LTE study are to continue longitudinal assessment of the efficacy and safety/tolerability of ALZ-801 over a total period of 4 years (2-year Core study plus 2 years of LTE).

Core study: ALZ-801 265 mg twice daily (BID) in the Core Study, Weeks 0-104

LTE year 1: ALZ-801 265 mg BID in the Core Study and the Long-Term Extension (LTE, Weeks 104-208)

LTE year 2: ALZ-801 265mg BID in the Core Study and LTE Year 1 (Weeks 104-156), and LTE Year 2 (Weeks 156-208)

研究设计

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

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

Experimental

ALZ-801 265 mg tablets once daily for two weeks and twice daily thereafter

干预措施: ALZ-801 (Drug)

结局指标

主要结局

Plasma Biomarker of Core AD Pathology

时间窗: Week 104

Percent change from baseline in p-tau181

Incidence, Nature, and Severity of Treatment Emergent Adverse events (TEAE)

时间窗: Week 108

Safety and tolerability as measured by incidence, nature and severity of treatment emergent adverse events (TEAE), serious TEAE, and TEAE leading to withdrawal.

Volumetric Magnetic Resonance Imaging (vMRI) Biomarker - Hippocampal Volume

时间窗: Weeks 104

Change from baseline in hippocampal volume measured in mm3

次要结局

  • Plasma Biomarkers of AD and Neurodegeneration(Weeks 104)
  • vMRI Biomarker - Ventricular volume and Cortical Thickness(Weeks 104, 156 and 208)
  • Additional CSF Biomarkers of AD Pathology and Neurodegeneration(Weeks 104)
  • Incidence, Nature, and Severity of Treatment Emergent Adverse events (TEAE)(Week 160 and week 212)
  • Volumetric Magnetic Resonance Imaging (vMRI) Biomarker - Hippocampal Volume(Week 156 and week 208)

研究者

发起方
Alzheon Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (4)

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Biomarker Effects of ALZ-801 in APOE4 Carriers With... | 临床试验