ClinicalTrials.gg
Status unknownNCT04897542Updated Sep 18, 2023

Gallium-68 NODAGA-JR11 PECT/CT in Neuroendocrine Tumors

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

The sponsor has not verified this record recently (last verified Sep 2023), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Dec 2020, registered May 2021).
Phase
Early Phase 1
Study type
Interventional
Enrollment
100
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
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Study summary

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.

Read the detailed description

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.

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Conditions studied

  • Neuroendocrine Tumors

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03

In context

Neuroendocrine Tumors

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 →

Lead sponsor

First Affiliated Hospital of Fujian Medical University is the lead sponsor of 96 studies on the registry; 55 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Written informed consent.

      • Patients of either gender, aged ≥ 18 years.
      • Histologically confirmed diagnosis of Metastatic, well-differentiated neuroendocrine tumor.
      • A diagnostic computed tomography (CT) or magnetic resonance imaging (MRI) of the tumor region within the previous 6 months prior to dosing day is available.
      • At least 1 measurable lesion based on RECIST v1.1.
      • 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)

      • Serum creatinine: within normal limits or \< 120 μmol/L for patients aged 60 years or older.
      • Calculated Glomerular filtration rate (GFR) ≥ 45 mL/min.

Exclusion criteria

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.

      • Presence of active infection at screening or history of serious infection within the previous 6 weeks.
      • Therapeutic use of any somatostatin analog, including long-acting Sandostatin (within 28 days) and short-acting Sandostatin (within 2 days) prior to study imaging. If a patient is on long-acting Sandostatina, then a wash-out phase of 28 days is required before the injection of the study drug. If a patient is on short-acting Sandostatin, then a wash-out phase of 2 days is required before the injection of the study drug.
      • Any neuroendocrine tumor-specific treatment between antagonist and agonist scans.
      • Prior or planned administration of a radiopharmaceutical within 8 half-lives of the radionuclide used on such radiopharmaceutical including at any time during the current study.
      • Pregnant or breast-feeding women.
      • Current history of any malignancy other than neuroendocrine tumor; patients with a secondary tumor in remission of > 5 years can be included.
      • Any mental condition rendering the patient unable to understand the nature, scope and possible consequences of the study, and/or evidence of an uncooperative attitude.
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Study design

Phase
Early Phase 1
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
100 participants (estimated)

Study arms

  • Experimental
    Patients will undergo a Gallium-68 NODAGA-JR11 PET/CT as well as a Gallium-68 DOTATATE PET/CT

    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

Interventions

  • DrugGallium-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.

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What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. 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

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Study locations

2 of 2 sites recruiting
  • Peking Union Medical College Hospital
    Beijing, Beijing Municipality 100000, China
    Recruiting
  • The First Affiliated Hospital of Fujian Medical University
    Fuzhou, Fujian 350000, China
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 18, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04897542
Lead sponsor
First Affiliated Hospital of Fujian Medical University
Responsible party
Weibing Miao, PhD (Director, Department of Nuclear Medicine, First Affiliated Hospital of Fujian Medical University) — Principal investigator
First posted
May 21, 2021
Start date
Dec 1, 2020
Primary completion
Dec 1, 2023 (estimated)
Completion
Dec 1, 2023 (estimated)
Last update
Sep 18, 2023

Study contacts

Weibing Miao, MD
Contact
miaoweibing@126.com
86-0591-87981618
Shaobo Yao, MD
Contact
yaoshaobo008@163.com
86-0591-87981619

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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