Liver Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with liver cancer (hepatocellular carcinoma)
- People who are planned to have surgery to remove part of the liver (hepatectomy)
- People whose liver is functioning at a level classified as Child-Pugh A or B (a measure of liver health — confirm with trial site)
- People whose liver cancer cells show high levels of a protein called GPC-3, confirmed before surgery
- People aged between 18 and 75 years, with a life expectancy of more than 6 months
- People who are willing and able to sign a consent form agreeing to take part
Who may not be able to join:
- People who have a known allergy to a dye called IRDye800 (used during the procedure)
- People who have taken part in another clinical trial within the past 3 months
- People who have been found to have another type of cancer
- People whose heart, lungs, kidneys, or other major organs are not functioning well enough
- People whose health means they would not be able to safely undergo liver surgery
- People who the trial researchers consider unsuitable for inclusion for any other reason
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 86-18201082715
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
HCC lesions
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.