Phase
Condition
Kidney Cancer
Cancer/tumors
Renal Cell Carcinoma
Treatment
[68Ga]Ga-DOTA-CAIX peptide
[68Ga]Ga-NOTA-CD70 antibody fragment
[68Ga]Ga-PSMA
Clinical Study ID
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Tumor subjects:
The subject or his/her legal representative is able to sign the informed consentform signed and dated;
Promise to abide by the research procedures and cooperate with the implementation ofthe whole process of research;
Adult subjects (aged 18 years or above), male or female;
Patients with clinically suspected or confirmed renal cell carcinoma (supportingevidence includes serum-related tumor markers, ultrasound, CT, MRI and other imagingdata and histopathological examinations, etc.), and are in good general condition;
Conform to specific laboratory test results;
Contraception for at least one month before screening for females in thechildbearing period, and commitment to use contraception throughout the study periodand continue until the specified time after the end of the study;
Other set selection criteria.
Healthy Subjects:
Fully understand and voluntarily sign the informed consent form;
Male or female, age 18-70 years old;
Male weight >=50.0kg, female weight >=45.0kg; Body mass index (BMI) within the rangeof 19.0~26.0kg/m^2 (including the cut-off value);
No history of chronic or serious diseases such as cardiovascular, liver, kidney,respiratory, blood and lymphatic, endocrine, immunologic, psychiatric,neuromuscular, gastrointestinal system, etc., within three years, and in goodgeneral health;
There is no abnormality in vital signs examination and physical examination;
Have no fertility plan during the trial and within 6 months after the end of thetrial and voluntarily take effective contraceptive measures and have no sperm andegg donation plans;
Able to communicate well with the investigator, and understand and comply with therequirements of the study.
Exclusion
Exclusion Criteria:
Tumor subjects:
Those who are unable to complete PET/MR or PET/CT examination (including inabilityto lie flat, claustrophobia, radiophobia, etc.);
Patients with known hypersensitivity to targeted PSMA, CAIX or CD70 PET imagingagents or synthetic excipients; The fasting blood glucose level before injection of [18F]FDG exceeded 11.0 mmol/L;
Patients who are pregnant or lactating;
Those who have other factors that are not suitable for participating in this test.
Healthy Subjects:
Any serious or unstable medical condition; Those who have acute illness before thestudy; Previous or existing malignancy;
Pregnant and lactating women;
Those who have undergone surgery within 6 months before the trial, which is judgedby the investigator to affect absorption, distribution, metabolism, and excretion;
Those who have used any drugs (including prescription drugs, over-the-counter drugs,and Chinese herbal medicines) within 2 weeks before the trial;
Participation in other research studies involving radioactive materials (within thepast 12 months);
Any other factors that affect the results of the study.
Study Design
Study Description
Connect with a study center
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan 1791247, Hubei 1806949 430022
ChinaActive - Recruiting

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