Phase 3 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 old
- People whose general health and ability to carry out daily activities meets a minimum standard (known as a KPS score of 70 or above — confirm with trial site if unsure what this means)
- People who have been diagnosed with hepatocellular carcinoma (a type of liver cancer) according to specific international diagnostic guidelines, and whose cancer falls into a particular stage category (BCLC A, B, or C — the trial site can confirm which stage applies)
- People who have at least one liver tumour that can be clearly and accurately measured using scans or imaging
- People whose cancer has been assessed by a panel of liver surgery specialists and agreed to be not suitable for surgical removal
- People who either have no liver scarring (cirrhosis), or whose liver scarring is mild and falls into a specific health classification (Child-Pugh class A)
- People whose recent blood test results meet all of the following levels: platelets at least 75,000/μL; haemoglobin at least 8.5 g/dL; total bilirubin no higher than 30 mmol/L; serum albumin at least 32 g/L; certain liver enzyme levels no more than 6 times the upper limit of normal; kidney function marker (creatinine) no more than 1.5 times the upper limit of normal; blood clotting measures within acceptable ranges; and neutrophil count above 1,500/mm³ (confirm all values with the trial site)
- People who are able to understand the trial procedures and are willing to sign a written consent form
Who may not be able to join:
- People who have had a significant episode of gastrointestinal (gut) bleeding within the 30 days before entering the trial
- People with a serious heart condition that would make treatment unsafe, such as certain irregular heart rhythms that require medication to control
- People who show signs that their liver is no longer functioning adequately, including fluid build-up in the abdomen, gut bleeding related to liver disease, or confusion caused by liver failure
- People who have a known HIV diagnosis
- People who have previously received an organ transplant
- People who are known or believed to be allergic to the study treatments or any other medicines used as part of the trial
- People who have a known tendency to bleed excessively
- People who have experienced a significant bleeding event (above a certain severity level) within the four weeks before the first dose of the study treatment
- People who have a wound, ulcer, or bone fracture that is not healing properly
- People who have tumours in the brain or central nervous system, including cancer that has spread to the brain
- People who are unlikely to be able to follow the treatment schedule and attend all required follow-up appointments
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.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
Overall survival
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Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.