NCT02336360已完成1 期
A Multicenter Study to Obtain Data to Assist in Radiation Dosimetry Calculations From Subjects Enrolled in Human Studies Employing 18F-AV-1451
Avid Radiopharmaceuticals1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2015年1月最近更新:
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
- 6
- 试验地点
- 1
- 主要终点
- Urine Analysis - Total Integrated Radioactivity Excreted in Urine
研究概览
简要总结
This study will obtain data from urine in subjects administered flortaucipir in an Avid-sponsored study to augment the calculation of radiation dosimetry estimates.
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
入排标准
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Subjects who passed screening in an Avid-sponsored study in which flortaucipir will be administered
排除标准
- •Subjects who have withdrawn informed consent
- •Investigator or sponsor believes it is in the best interest of the subject to be removed from the trials
研究组 & 干预措施
Urine Analysis
Experimental
Urine will be collected from subjects administered flortaucipir in an Avid-sponsored study to determine the amount of radioactivity excreted in urine.
干预措施: Flortaucipir F18 (Drug)
结局指标
主要结局
Urine Analysis - Total Integrated Radioactivity Excreted in Urine
时间窗: 0-360 minutes post injection
Total integrated radioactivity excreted in urine over time will be determined to augment previous radiation dosimetry calculations.
次要结局
未报告次要终点
研究者
研究点 (1)
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