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)

Loading locations...

相似试验

Evaluation of Flortaucipir PET Signal and Cognitive... | 临床试验