18F-T2 PET/CT Imaging for CAIX Positive Solid Tumors

Recruiting now · Not applicable

Conditions studied: Clear Cell Renal Cell Cancer (ccRCC), Urothelial Carcinoma (UC), Colorectal Cancer, Cervical Cancer, Ovarian Cancer, Head and Neck Cancer, Hepatocellular Carcinoma (HCC), Cholangiocarcinoma, Non Small Cell Lung Cancer, Small Cell Lung Cancer, Breast Cancer, Pancreatic Cancer, Endometrial Cancer, Von Hippel Lindau Disease

In brief

The goal of this clinical trial is to evaluate the diagnostic value of CAIX protein specific probe 18F-T2 in PET/CT imaging in participants with solid tumors. It will also assess the safety, tolerability and radiation dosimetry of 18F-T2.

Key facts

Study ID

NCT07557225

Run by

Peking University First Hospital

People needed

200

Starts

2026-04-27

Expected to finish

2029-03-01

Last updated by the study team

2026-05-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• All participants must meet the following criteria:
• Written and voluntarily given Informed Consent.
• Male or female ≥18 years of age at time of consent.
• Have the capacity to understand the study and be willing and able to comply with all protocol requirements.
• Participants with histologically confirmed or suspected tumors of the following types, but not limited to:
• Clear Cell Renal Cell Cancer; Urothelial Carcinoma; Colorectal Cancer; Cervical Cancer; Ovarian Cancer; Head and Neck Cancer; Hepatocellular Carcinoma; Cholangiocarcinoma; Non Small Cell Lung Cancer; Small Cell Lung Cancer; Breast Cancer; Pancreatic Cancer; Endometrial Cancer; Von Hippel Lindau Disease.

You may not qualify if…

• Participants will be excluded from participation in the study if one or more of the following criteria are met:
• Have any serious non-malignant disease (e.g., psychiatric, infectious, autoimmune or metabolic) that may interfere with the objectives of the study or with the safety or compliance of the participant, as judged by the Investigator.
• Have a mental impairment that may compromise the ability to give Informed Consent and comply with the requirements of the study.
• Be a female who is pregnant or breastfeeding.

Where it is running

• Peking University First Hospital — Beijing, Beijing Municipality, China (enrolling)

Full record on ClinicalTrials.gov

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