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临床试验/NCT05728515
NCT05728515已完成早期 1 期

Pilot Clinical Evaluation of a Small-molecule Carbonic Anhydrase IX Targeting PET Tracer in Clear Cell Renal Cell Carcinoma

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 3 人开始时间: 2021年12月25日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
早期 1 期
状态
已完成
入组人数
3
试验地点
1
主要终点
Tumor uptake of 68Ga-NY104

研究概览

简要总结

The goal of this pilot clinical trial is to see the potential application of a CAIX targeted PET. tracer in patients with clear cell renal cell carcinoma. The main question[s] it aims to answer are:

  • The biodistribution of the PET tracer
  • Whether RCC lesions can be identified by the PET tracer Participants will undergo 68Ga-NY104 PET/CT scan and images will be reviewed by nuclear medicine specialists.

详细描述

PET/CT imaging of three patients using 68Ga-NY104 for medical reasons will be performed. Patients received an intravenous injection of 68Ga-NY104. Images will be obtained at 0.5 h, 1 h, and 2 h after injection. A comparative 18F-FDG PET/CT scan will also be performed if necessary. The study will be carried out on a time-of-flight PET/CT scanner. SUVmax and SUVmean of normal organs and lesions, as well as tumor-to-background ratios, will be quantitatively assessed using a region-of-interest technique.

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

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Confirmed or suspected metastatic ccRCC
  • Written informed consent provided for participation in the trial
  • In the opinion of investigator, willing and able to comply with required study procedures.

排除标准

  • Patients on VEGF TKI treatment < 1 week before 68Ga-NY104 PET/CT. TKI is known to affect girentuximab binding in patients with ccRCC. If patients were on VEGF TKI treatment, such as sunitinib, sorafenib, cabozantinib, pazopanib, or lenvatinib, a washout of one week before 68Ga-NY104 PET/CT is required.
  • Pregnancy or breastfeeding.
  • Severe claustrophobia.

研究组 & 干预措施

PET scan

Experimental

Patients will receive an intravenous injection of 68Ga-NY104

干预措施: 68Ga-NY104 (Drug)

结局指标

主要结局

Tumor uptake of 68Ga-NY104

时间窗: From study completion to 2 hour after completion

Uptake measured by SUVmax and SUVmean in suspected tumor lesions

Biodistribution of 68Ga-NY104 in normal organs

时间窗: From study completion to 2 hour after completion

Uptake measured by SUVmax and SUVmean in normal organs using a region-of-interest technique

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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