Phase
Condition
Carcinoma
Treatment
18F-NY104 PET/CT
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- (1)Capable of understanding and voluntarily signing the informed consent form; ableto complete the trial in accordance with the protocol requirements; (2)Age 18-75years; no gender restrictions; (3)Clinically diagnosed/suspected as renal cellcarcinoma or clinically diagnosed/suspected recurrence/metastasis after RCCtreatment; (4)At least 1 measurable solid lesion in the subject, which can beaccurately and continuously measured using modified RECIST criteria (version 1.1); (5)ECOG performance status score of 0-2; (6)Laboratory parameters must meet:
Hematology: WBC ≥4.0×10⁹/L or neutrophils ≥1.5×10⁹/L, PLT ≥100×10⁹/L, Hb ≥90g/L; PT or APTT ≤1.5×ULN (upper limit of normal);
Liver and kidney function: T-Bil ≤1.5×ULN, ALT/AST ≤2.5×ULN or ≤5×ULN (forsubjects with liver metastasis), ALP ≤2.5×ULN (if bone or liver metastasispresent, ALP ≤4.5×ULN); BUN ≤1.5×ULN, SCr ≤1.5×ULN;
Other routine tests within normal ranges or deemed acceptable by theinvestigator; (7)Expected survival ≥12 weeks; (8) Female subjects: Effectivecontraception (defined as sterilization, intrauterine hormone device, condoms,contraceptives/agents, abstinence, or partner vasectomy) must be used duringthe study and for 6 months post-study; Male subjects: Agreement to usecontraception during the study and for 6 months post-study.
Exclusion
Exclusion Criteria:
Recovery from major trauma (including surgery) within 4 weeks prior to studyexamination;
Patients with systemic or local severe infections or other serious comorbidities;
Severe hepatic or renal dysfunction;
Refusal to participate in this clinical study;
Patients with a history of allergy to any component of the imaging agent (includingantibodies) or allergic constitution;
Childbearing-aged male or female subjects who cannot adopt effective contraception;
Women planning pregnancy, currently pregnant, or lactating;
Patients unable or unwilling to undergo PET/CT scanning;
Other subjects deemed ineligible by the investigator.
Study Design
Study Description
Connect with a study center
The Affiliated Hospital of Qingdao University
Qingdao, Shandong
ChinaActive - Recruiting

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