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NCT Number: NCT06519760

68Ga-C1 PET/ CT Imaging in Clear Cell Renal Cell Carcinoma

The goal of this clinical trial is to evaluate the diagnostic value of CAIX protein specific probe 68Ga-C1 in PET/CT imaging in clear cell renal cell carcinoma patients. It will also learn about the safety, tolerability and radiation dosimetry of 68Ga-C1.

Researchers will compare the diagnostic value of 68Ga-C1 PET/CT and 18F-FDG PET/CT in Chinese patients with indeterminate renal masses or confirmed clear cell renal cell carcinoma.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Peking University First Hospital

Beijing, Beijing Municipality, 100034, China

Location status: Recruiting

Location contact

About this study

Carbonic anhydrase IX (CAIX) is a transmembrane protein which is highly expressed in approximately 95% of clear cell renal cell carcinomas, and it is closely related to tumor progression, patients prognosis and treatment response. Here, we developed a CAIX specific small molecule probe 68Ga-C1, which has shown a good diagnostic accuracy in PET/CT imaging in our preclinical mouse model of clear cell renal cell carcinoma. This enables high-contrast imaging of clear cell renal carcinoma, providing a new imaging method for the precise diagnosis of clear cell renal carcinoma. In this clinical trail, we will compare the diagnostic value of 68Ga-C1 PET/CT and 18F-FDG PET/CT in Chinese patients with indeterminate renal masses or confirmed clear cell renal cell carcinoma.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed written informed consent;
  • Age ≥18;
  • Patients with confirmed or suspected clear cell renal cell carcinoma;
  • Expected survival ≥6 months.

Exclusion criteria

  • Renal mass is known to be a metastasis of another primary tumor;
  • Have other malignancies that require treatment;
  • Have received chemotherapy, radiotherapy, or immunotherapy within 4 weeks;
  • Renal insufficiency with glomerular filtration rate (GFR) ≤ 60 mL/min/1.73 m²;
  • Pregnant and lactating women or female patients plan to become pregnant within 6 months;
  • Uncontrolled psychiatric disorders;
  • Vulnerable population (e.g., being in detention) or have a serious non-malignant disease (e.g., infectious disease, autoimmune disease, or metabolic disease).

Treatment and study plan

68Ga-C1

Drug

68Ga-C1 is injected intravenously with a dose of 0.05-0.10 mCi/kg

Other names: CAIX specific PET imaging

Primary outcomes

  1. The diagnostic efficacy of 68Ga-C1 PET/CT in the evaluation of clear cell renal cell carcinoma

    Time frame: 1 year

    Compare the standardized Uptake Value (SUV) of lesions on 68Ga-C1 and 18F-FDG PET/CT

  2. The diagnostic efficacy of 68Ga-C1 PET/CT in the evaluation of malignant tumors

    Time frame: 1 year

    Compare the number of lesions detected by 68Ga-C1 and 18F-FDG PET/CT, based on the pathology or clinical follow-up as gold standard.

Secondary outcomes

  1. The dosimetry of 68Ga-C1

    Time frame: 1 year

    Research on the dose distribution of 68Ga-C1 in healthy volunteers and cancer patients by 1-hour dynamic PET/CT acquisition and analyze by the dosimetry software

  2. Quantitative evaluation of 68Ga-C1

    Time frame: 1 year

    Evaluation of quantitative parameters of 68Ga-C1, such as time-activity curve.

  3. Correlation with pathological expression

    Time frame: 1 year

    Analyze CAIX expression at the imaging level in combination with CAIX expression in pathological specimens

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Peking University First Hospital

Other

Registry information

Official study title

Evaluation of Diagnostic Value of 68Ga-C1 PET/ CT Imaging in Clear Cell Renal Cell Carcinoma

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Jul 25, 2024
Registry last updated
Nov 7, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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