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临床试验/NCT06688188
NCT06688188招募中1 期

68Ga-JH12 PET/CT: Dosimetry and Biodistribution Study in Patients With Various Cancers

First Affiliated Hospital of Fujian Medical University1 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2024年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
5
试验地点
1
主要终点
safety and tolerability

研究概览

简要总结

68Ga-JH12 is a novel radiotracer targeting C-X-C motif chemokine receptor 4 (CXCR4). In this study, we observed the safety, biodistribution, and radiation dosimetry of 68Ga-JH12 in patients with different types of cancer.

详细描述

C-X-C motif chemokine receptor 4 (CXCR4) is highly expressed in patients affected with malignant tumors and ex-vivo analyses provided evidence that the expression level on the tumor cell surface is tightly linked to the proliferation index. In recent years, the diagnostic PET agent 68Ga-Pentixafor targeting this chemokine receptor has been extensively validated in haematological malignancies and solid tumors. 68Ga-JH12, a novel radiopharmaceutical targeting CXCR4, demostrated high stability in vitro and in vivo, and can accumulate specifically in tumors with high binding affinity, safety, and selectivity in preclinical studies. In this study, the safety, biodistribution, and radiation dosimetry of 68Ga-JH12 in patients with Various Cancers were observed to evaluate the dosimetric characteristics of 68Ga-JH12.

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 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Various solid tumors with available histopathological findings
  • Signed informed consent

排除标准

  • pregnant or lactational women
  • who suffered from severe hepatic and renal insufficiency

研究组 & 干预措施

dynamic PET scans

Experimental

PET imaging will begin at 3 minutes, 15 minutes, 30min minutes, 60 minutes and 150 minutes after injection.

干预措施: 68Ga-JH12 (Drug)

结局指标

主要结局

safety and tolerability

时间窗: up to 1 week

Hematologic status, liver function, renal function and General vital signs were recorded before and 1 week after administration of radiopharmaceutical. Adverse events were categorized using the Common Toxicity Criteria for Adverse Events 5.0.

次要结局

  • Dosimetry of normal organs and tumors(From right after tracer injection to 150 minutes at post-injection)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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68Ga-JH12 PET/CT: Dosimetry and Biodistribution Study | 临床试验