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 aged between 18 and 75 years
- People who have been diagnosed with hepatocellular carcinoma (a type of liver cancer), confirmed by imaging, tissue sample, or cell testing
- People whose liver cancer has spread into a specific part of a major liver blood vessel, classified as Type I or Type II (confirm with trial site for exact classification)
- People whose liver is functioning at a level doctors classify as "Child-Pugh class A" (a measure of liver health — confirm with trial site)
- People who are largely able to carry out daily activities, with little or no limitation due to illness (rated 0 or 1 on a standard medical scale)
- People who have not previously received any systemic (whole-body) drug treatment for their liver cancer
- People whose blood counts and organ function meet minimum health thresholds set by the trial (confirm with trial site for specific values)
- People who have at least one measurable tumour in the liver that can be tracked during the trial
Who may not be able to join:
- People whose liver cancer is spread diffusely throughout the liver rather than in defined tumours
- People whose liver cancer is a specific subtype, including cholangiocarcinoma, fibrolamellar, sarcomatoid, or mixed hepatocellular/cholangiocarcinoma, confirmed by tissue testing
- People whose cancer has spread to areas outside the liver
- People for whom the trial's treatment procedures would be medically inadvisable, as determined by the trial doctors
- People who have a history of serious bleeding events (above a certain severity level) in the four weeks before joining the trial
- People with an active or past autoimmune disease or a condition affecting the immune system
- People with untreated or incompletely treated enlarged veins in the oesophagus or stomach that are bleeding or carry a high risk of bleeding
- People who had a bleeding event from oesophageal or stomach varices within the six months before starting the trial
- People with evidence of significant blood clotting problems or difficulty controlling bleeding
- People who are pregnant or breastfeeding
- People with significant heart or cardiovascular disease
- People with a severe active infection, such as active tuberculosis
- People with serious ongoing medical conditions (confirm with trial site for specifics)
- People who have previously had an organ or cell transplant
- People who have another cancer that is not curable
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
Principal Investigator: Mingsheng Huang, M.D. & Ph.D., Department of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-sen University
Phone: +86-02085253416
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
Overall survival (OS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.