An Early Phase 1 interventional study of Gallium-68 NODAGA-JR11 in Neuroendocrine Tumors, sponsored by First Affiliated Hospital of Fujian Medical University. Status unknown at 2 sites in China. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2023-09-18.
Sponsored by First Affiliated Hospital of Fujian Medical University · Early Phase 1, Interventional, and Diagnostic
NODAGA-JR11 is a novel somatostatin receptor antagonist, while Gallium-68 DOTATATE is a typical somatostatin receptor agonist. This study is to evaluate the lesion detection ability of Gallium-68 NODAGA-JR11 for the diagnostic imaging of metastatic, well-differentiated neuroendocrine tumors using positron emission tomography / computed tomography (PET/CT).
The results will be compared between antagonist Gallium-68 NODAGA-JR11 and agonist Gallium-68 DOTATATE in the same group of patients.
Patients with histologically confirmed metastatic, well-differentiated neuroendocrine tumors will be recruited in this study.
Each patient received an intravenous injection of 68Ga-DOTATATE (40ug/150-200MBq) on the first day and 68Ga-NODAGA-JR11 (40ug/150-200MBq) on the second day. Whole-body PET/CT scans were performed at 40-60 min after injection on the same scanner. Physiologic normal-organ uptake, lesion numbers, and lesion uptake were compared.
682 studies on the registry are indexed under Neuroendocrine Tumors; 164 are open to participants now.
This study's planned enrollment of 100 is above the median of 42 across 470 interventional studies indexed under Neuroendocrine Tumors.
Browse Neuroendocrine Tumors studies →First Affiliated Hospital of Fujian Medical University is the lead sponsor of 96 studies on the registry; 55 are open to participants now.
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Written informed consent.
Blood test results as follows (White blood cell: ≥ 3*10\^9/L, Hemoglobin:
≥ 8.0 g/dL, Platelets: ≥ 50x10\^9/L, Alanine aminotransferase / Aspartate aminotransferase / Alkaline phosphatase: ≤ 5 times upper limit od normal (ULN), Bilirubin: ≤ 3 times ULN)
Exclusion Criteria:
Known hypersensitivity to Gallium-68, to NODAGA, to JR11, to TATE or to any of the excipients of Gallium-68 NODAGA-JR11 or Gallium-68 DOTATATE.
Each patient receive a single intravenous injection of Gallium-68 DOTATATE (40ug/150-200MBq) PET/CT, and undergo PET/CT scan at 40-60 min post-injection. All patients have to do a Gallium-68 NODAGA-JR11 PET/CT scan (40ug/150-200MBq, 40-60 min post-injection) for comparison on the next day of DOTATATE scan.
Drug: Gallium-68 NODAGA-JR11
Each patient receive a single intravenous injection of Gallium-68 NODAGA-JR11 (40ug/150-200MBq) PET/CT, and undergo PET/CT scan at 40-60 min post-injection.
Standard uptake value (SUV)
Determination of SUV for detected lesions and discernible organs of 68Ga-NODAGA-JR11 and 68Ga-DOTATATE scan.
Time frame: From right after tracer injection to 2-hours post-injection
Lesion numbers
Determination of lesion numbers of 68Ga-NODAGA-JR11 and 68Ga-DOTATATE scan.
Time frame: From right after tracer injection to 2-hours post-injection
Plan to share: No
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This study is status unknown, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.
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First Affiliated Hospital of Fujian Medical University