NCT06937112招募中不适用
Clinical Application of a Novel 18F Labeled Fibroblast Activation Protein (FAP) Targeted Molecular Probe in Early Tumor Diagnosis
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- SUVmax of lesion uptake value
研究概览
简要总结
Evaluate the safety of the novel FAP targeted molecular probe 18F-FAPI-YQ104 labeled with radioactive isotopes in clinical applications and verify its effectiveness in tumor diagnosis.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 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
- 否
入选标准
- •Volunteer for the trial, with the patient or their legal guardian signing the informed consent form;
- •Volunteers are not limited by gender, and the age range is from 18 to 75 years old, including both ends;
- •Other imaging examination methods (CT, MRI, etc.) revealed tumor occupying lesions;
- •Patients with lung cancer, thyroid cancer, pancreatic cancer, melanoma, and neuroendocrine tumors who can obtain the final pathological results.
- •Kidney: GFR > 50 ml/min, ERPF > 280 ml/min, platelet count (PLT) > 75,000/μL, white blood cell (WBC) > 3,000/μL, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels less than 3 times the normal value.
排除标准
- •Individuals with a history of allergies to similar drugs (drugs with similar chemical or biological components to FAPI), allergic constitution, or current allergic diseases;
- •Those who are currently conducting clinical research on other drugs or have participated in any clinical research on drugs (excluding vitamins and minerals);
- •There are other clinical problems that are difficult to control (such as HIV, hepatitis C virus infection or active hepatitis B, or other serious chronic infections and serious mental, neurological, cardiovascular, respiratory and other system diseases);
- •Red blood cell RBC<4 × 1012, white blood cell WBC<3 × 109, hemoglobin<110g/L, PLT<75000×109;
- •Significant abnormalities in liver and kidney function, with GFR less than 50 ml/min;
- •Tumor burden greater than 50%, or significant spinal cord compression;
- •Expected survival period is less than six months; Chemotherapy within June;
- •Having severe acute comorbidities or severe refractory mental disorders;
- •Pregnant and lactating women (where pregnancy is defined as a positive urine pregnancy study);
- •Patients whose physical condition is not suitable for radiation examination;
- •Other situations that researchers consider unsuitable for participating in the experiment.
结局指标
主要结局
SUVmax of lesion uptake value
时间窗: 60 minutes after administration
次要结局
未报告次要终点
研究者
Feng Wang
Chief physician
Nanjing First Hospital, Nanjing Medical University
研究点 (1)
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