Life sciences · Observational Study
ClinicalTrials.gov · September 28, 2026
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Observational Study.
No findings were extractable from the material analysed.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
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Registry record from ClinicalTrials.gov (NCT07039474). This is a study registration, not published results. Lead sponsor: Peking University First Hospital. Recruitment status: RECRUITING. Study type: OBSERVATIONAL. Enrollment: 120 participants (ESTIMATED). Conditions: Solid Tumor Malignancies, Hematologic Cancer, Lung Cancer, Esophagus Cancer, Breast Cancer, Kidney Cancer, Stomach Cancer, Lymphoma. Interventions: DRUG: 18F-G1. Primary outcome measures: Number of participants with 18F-G1-related adverse events (AEs). , 3 days after the injection of 18F-G1; Tumor uptake of 18F-G1 , 40-60 minutes after the injection of 18F-G1; Liver uptake of 18F-G1 , 40-60 minutes after the injection of 18F-G1; Lung uptake of 18F-G1 , 40-60 minutes after the injection of 18F-G1; Kidney uptake of 18F-G1 , 40-60 minutes after the injection of 18F-G1; the granzyme B specificity of 18F-G1 , 3 years; Assessing the early predictive value of 18F-G1 PET/CT for immunotherapy response. , 6 months. Brief summary: The purpose of this study is to explore the effectiveness of 18F-G1 PET/CT in patients with solid tumors and hematological malignancies receiving immunotherapy