Phase 2 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:
- You are willing to participate, agree to follow-up visits, and have signed a written consent form
- You are between 18 and 80 years old (any gender)
- You have been officially diagnosed with hepatocellular carcinoma (a type of liver cancer) and have had a tissue sample (biopsy) taken to confirm the diagnosis
- You have at least one tumor that is large enough to be measured on a CT scan, based on specific size guidelines
- You have not received any previous systemic (whole-body) treatment for this cancer
- Your liver cancer is at a certain stage (stages IIa through IIIb based on a Chinese staging system) (confirm with trial site)
- Your cancer is considered "high tumor load," meaning either the number and size of tumors meets a specific threshold, or the cancer has spread into major blood vessels near the liver (confirm with trial site)
- Your liver is functioning at a level rated as Child-Pugh grade A or B with a score of 5–8 (confirm with trial site)
- Your general physical health is rated 0 or 1 on a standard activity scale (meaning you are fully active or have only minor limitations)
- You are expected to live for at least 12 weeks
- If you have an active hepatitis B infection, it is either at a low level or has been treated with antiviral medication for at least one week before starting the trial
- Your blood counts and organ function (blood, liver, and kidney) meet specific minimum levels set by the trial
- If you are a woman who could become pregnant, you have had a negative pregnancy test within 7 days before joining, and you agree to use contraception during the trial and for 8 weeks after the last dose; if you are a man, you agree to use contraception or have had a sterilisation procedure during the trial and for 8 weeks after the last dose
Who may not be able to join:
- You are pregnant or currently breastfeeding
- You have an autoimmune disease, have had an organ or stem cell transplant, or have another active cancer (except certain previously cured skin or cervical cancers)
- You have a mental illness or are unable to cooperate with treatment
- You have taken part in another clinical trial in the past 3 months
- You have received local treatments for your cancer (such as surgery, radiation, or similar procedures) within the past month
- You have had a serious blood clot or stroke event (such as a blood clot in the lung or leg, or a mini-stroke) within the past 6 months — not including blood clots in the portal vein, which are allowed
- You have taken immune-suppressing medications or high-dose steroids within the past 14 days
- You have had bleeding from veins in your oesophagus or stomach within the past month
- You have serious problems with blood clotting that cannot be corrected, or a platelet count that is too low
- You have severe fluid build-up in the abdomen that cannot be controlled
- You have an active infection, especially in the bile ducts
- You have serious failure of the liver, kidneys, heart, lungs, brain, or other major organs
- You have previously used targeted therapy drugs, PD-1 antibody treatments, or similar medications
- You have high blood pressure that cannot be brought under control with medication (above 140/90 mmHg)
- You have a significant heart condition, such as a heart attack, serious irregular heartbeat, or poor heart function
- You have significant levels of protein in your urine
- You are unable to swallow tablets or have a condition that affects how your body absorbs medication
- You have any other condition that the trial doctor believes could put you at risk or prevent you from completing the trial
- You do not wish to have a tissue biopsy to confirm your diagnosis
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: Zhong Tang, Nanping First Hospital of Fujian Province
Phone: 13805066904
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
Objective response rate (ORR)
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.