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New treatment option for Carbonic Anhydrase IX
Official title 68Ga-C1 PET/ CT Imaging in Clear Cell Renal Cell Carcinoma
ClinicalTrials.gov ID: NCT06519760
What this study is testing
What is 68Ga-C1?
68Ga-C1 is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for carbonic anhydrase ix.
Also referred to as CAIX specific PET imaging.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Signed written informed consent；
- Age ≥18；
- Patients with confirmed or suspected clear cell renal cell carcinoma;
- Expected survival ≥6 months.
You likely can't join if
- 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;
See the full eligibility criteria
- Signed written informed consent；
- Age ≥18；
- Patients with confirmed or suspected clear cell renal cell carcinoma;
- Expected survival ≥6 months.
- 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).
The study team makes the final eligibility decision.
Where it's taking place
- Beijing, Beijing Municipality, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Beijing, Beijing Municipality, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.