跳至主要内容
临床试验/NCT03901105
NCT03901105已完成3 期

Evaluation of the Relationship Between Baseline Flortaucipir PET Signal and Cognitive Change in Subjects With Early Alzheimer's Disease Participating in the I8D-MC-AZES Protocol Addendum D5010C00009 (2.1) (Tau Imaging)

Avid Radiopharmaceuticals1 个研究点 分布在 1 个国家目标入组 205 人开始时间: 2019年3月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
205
试验地点
1
主要终点
Risk Ratio for AD Symptom Progression on CDR-SB

研究概览

简要总结

This study will evaluate whether visual interpretation of flortaucipir-PET (positron emission tomography) scans, examining patterns of tracer uptake at baseline, can predict the rate of clinically-meaningful cognitive decline due to AD after 18 months. All scans are acquired from cohorts of a previously completed study, I8D-MC-AZES (NCT02245737, lanabecestat, Eli Lilly and Company sponsor).

研究设计

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

盲法说明

PET scans were obtained in an open-label fashion.

入排标准

年龄范围
55 Years 至 85 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

Flortaucipir PET Scan

Experimental

No study drug will be administered. Scans previously acquired from Study I8D-MC-AZES (NCT02245737, Eli Lilly and Company sponsor) will be read by independent, blinded readers.

干预措施: flortaucipir F18 (Drug)

Flortaucipir PET Scan

Experimental

No study drug will be administered. Scans previously acquired from Study I8D-MC-AZES (NCT02245737, Eli Lilly and Company sponsor) will be read by independent, blinded readers.

干预措施: Brain PET Scan (Procedure)

结局指标

主要结局

Risk Ratio for AD Symptom Progression on CDR-SB

时间窗: Within 18 months of scan

Baseline flortaucipir F 18 PET imaging results were determined by majority read (see Baseline Characteristics for description). Clinically meaningful deterioration (CMD) was defined for the primary endpoint as a worsening of the Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) score of one point or more. The clinical dementia rating (CDR) examines 6 categories of cognitive functioning domains. Each domain is scored on a scale ranging from 0 to 3 (including 0.5). A CDR-SB was generated as the sum of the values in each of the 6 domains. The CDR-SB sum scores range from 0 to 18, with higher scores indicating greater cognitive impairment and a 1 point worsening is considered a clinically significant symptom change.

次要结局

  • Mean Change in Cognitive/Functional Assessments(baseline and 18 months)
  • Inter-Reader Reliability of Reader Interpretation of Flortaucipir F 18 PET Imaging(baseline scan)
  • Risk Ratio for AD Symptom Progression on Various Clinical Measures(Within 18 months of scan)

研究者

发起方
Avid Radiopharmaceuticals
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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