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临床试验/NCT06716788
NCT06716788尚未招募不适用

Development and Clinical Translation of Protein-losing Enteropathy (PLE) Imaging PET Probe

Peking University Cancer Hospital & Institute1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
Standard Uptake Value Value

研究概览

简要总结

In this project, based on the DTPA-HAS kit, investigators plan to develop a positron nuclide 68Ga labeled DTPA-HSA molecular probe in order to obtain high sensitivity, signal-to-noise ratio and high-resolution PET/CT imaging images, aiming to find the specific site of intestinal leakage while diagnosing Protein-Losing Enteropathy (PLE), and analyze the pathological mechanism of intestinal leakage in combination with pathology, so as to provide molecular imaging guidance for the treatment of PLE patients. PLE is a rare gastrointestinal protein-losing syndrome, and the radiopharmaceutical 99mTc-DTPA-HSA (99mTc-human serum albumin) approved by the State Food and Drug Administration has the diagnostic ability of protein-losing enteropathy (PLE), but due to the low resolution of SPECT/CT, the image clarity and signal-to-noise ratio need to be improved, it is a classic probe in the last century, unable to meet the existing clinical needs.

详细描述

This project developed a a new type of nuclide Ga-68 labeled DTPA-HSA probe, and with the inherent advantages of this nuclear medicine department, it has promoted the formulation of the production filing standard of the drug, and obtained the 68Ga-HSA injection that can be used for preclinical research and meets the clinical standards. Clinical research on 68Ga-HSA PET/CT imaging was carried out to provide a basis for the diagnosis and treatment of PLE patients.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with digestive system tumors;
  • Presence of hypoproteinemia or clinical manifestations of hypoplasma protein;
  • Serum albumin <30 g/L, AAT>80 ml/d;
  • Measurable lesions in imaging;
  • Predicted survival greater than 3 months;

排除标准

  • Severe hepatic or renal dysfunction;
  • Pregnant or nursing;
  • Known allergy to the investigational drug or its excipients in study;
  • Unable to comply with the PET/CT imaging procedures;
  • Claustrophobia or other psychiatric disorders;
  • Other conditions deemed unsuitable for participation in the trial;

研究组 & 干预措施

68Ga-HSA PET/CT in participants with hypoproteinemia

Participants who are with hypoproteinemia will be injected with 2.22 MBq/kg body weight of 68Ga-HSA in one dose intravenously and then undergo PET/CT scan within 1 h.

干预措施: 68Ga-HSA (Drug)

结局指标

主要结局

Standard Uptake Value Value

时间窗: 1 year

The standardized uptake value(SUV) of 68Ga-HSA in suspected PLE lesions measured by the PET/CT

SUVR

时间窗: 1 year

Ratio of the SUV of 68GA-DTPA-HSA in the suspected PLE lesions to the SUV of 68Ga DTPA-HSA in the normal tissues corresponding to the PLE (SUVR)

次要结局

未报告次要终点

研究者

发起方
Peking University Cancer Hospital & Institute
申办方类型
Other
责任方
Sponsor

研究点 (1)

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