Study on the Clinical Application Value of PET Imaging Targeting GPC3 in Hepatocellular Carcinoma
Recruiting
Early Phase 1Interventional Study
Malignant Neoplasm of Liver
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 – 65
Sex
Any
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Diagnostic
Participants needed
100 (estimated)
Sponsor
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Other
Who this trial is looking for
This trial is looking for adults with liver cancer or healthy volunteers. Participants will undergo special imaging tests to help diagnose and understand liver cancer better.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old
I have been diagnosed with liver cancer or I am a healthy volunteer
I am willing to sign the consent form
I can follow the visit and treatment schedule
I have a history of liver cancer that has come back after treatment
You may not be able to join if
I am pregnant or breastfeeding
I cannot sign the consent form
I have serious system diseases or electrolyte issues
I am allergic to imaging agents used in the study
My blood sugar is higher than 11.0 mmol/L before the test
I cannot complete the imaging tests
I have poor compliance or other factors that may interfere with the study
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This is a diagnostic study. Patients were recruited from patients with clinically suspected or confirmed hepatocellular carcinoma and healthy volunteers were recruited for PET/or PET/CT imaging targeting a GPC3-specific probe (in the case of 68Ga-NOTA-aGPC3-scFv) , to observe the reaction of volunteers and patients after injection of drugs, to evaluate the pharmacokinetics in vivo and the efficacy…
This is a diagnostic study. Patients were recruited from patients with clinically suspected or confirmed hepatocellular carcinoma and healthy volunteers were recruited for PET/or PET/CT imaging targeting a GPC3-specific probe (in the case of 68Ga-NOTA-aGPC3-scFv) , to observe the reaction of volunteers and patients after injection of drugs, to evaluate the pharmacokinetics in vivo and the efficacy of diagnosis and staging, and to perform PET CT imaging in patients with contraindications. General Information, clinical data, blood routine, liver and renal function, and other imaging data were collected. The final diagnosis was based on the histopathology of biopsy or surgical specimens.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 1: Voluntarily participate and the person or their legal representative can sign an informed consent form
* 2: Adult patients (18 years of age or older), regardless of gender
* 3: Patients with newly diagnosed hepatocellular carcinoma with high clinical suspicion or confirmati…
Inclusion Criteria:
* 1: Voluntarily participate and the person or their legal representative can sign an informed consent form
* 2: Adult patients (18 years of age or older), regardless of gender
* 3: Patients with newly diagnosed hepatocellular carcinoma with high clinical suspicion or confirmation (supporting evidence including imaging data and histopathologic examination, etc.) who agree to undergo histopathologic examination (if not performed prior to imaging) or/and 18F-FDG PET imaging
* 4: Healthy volunteer
* 5: Patients with a history of hepatocellular carcinoma, remission and recurrence after treatment
* 6: Willing and able to follow schedule visits, treatment plans and laboratory tests
Exclusion Criteria:
* 1: Pregnant or lactating patients
* 2: The patient or their legal representative is unable or unwilling to sign the informed consent form
* 3: Acute systemic diseases and electrolyte disorders
* 4: Patients who are known to be allergic to GPC3 imaging agents or synthetic excipients
* 5: Fasting blood glucose levels exceeding 11.0 mmol/L before injection of 18F-FDG
* 6: Individuals who are unable to complete PET/MR or PET/CT examinations (including inability to lie flat, claustrophobia, radiation phobia, etc.)
* 7: Researchers believe that compliance is poor or there are other unfavorable factors for participating in this experiment
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