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 must be at least 18 years old.
- You must be willing and able to sign a consent form agreeing to take part.
- You have been diagnosed with liver cancer (hepatocellular carcinoma/HCC) that has spread or cannot be removed by surgery, confirmed by a tissue sample or by standard diagnostic criteria used by liver disease specialists.
- Your liver cancer got worse after receiving a specific type of previous treatment combining an immunotherapy drug (anti-PD1/PD-L1) and a drug called bevacizumab.
- You have at least one tumor that can be measured on a scan, which has either not been treated locally before, or has grown again after local treatment.
- Your liver function and overall health fall within acceptable ranges as measured by specific scoring systems (Child-Pugh score of 5–7 and an activity/fitness score of 2 or less on the ECOG scale).
- If you have a chronic hepatitis B infection, your virus levels must be very low (below 100 IU/mL at screening) and you must already be on antiviral medication.
- Your doctors expect you to live for at least 12 weeks.
- Your blood counts, liver enzymes, and kidney function must meet specific acceptable levels (confirm with trial site for exact values).
- If you are a woman who could become pregnant, you must have a negative pregnancy test within 7 days before starting the trial.
- You must be willing and able to follow all trial requirements, including attending appointments, following contraception guidelines, and completing all follow-up visits.
Who may not be able to join:
- You have a specific rare subtype of liver cancer (fibrolamellar HCC, sarcomatoid HCC, or a mixed type involving bile duct cancer).
- You are on a waiting list for a liver transplant or have very advanced liver disease.
- You have a significant history of heart disease or have had a serious gastrointestinal bleed within the past 4 weeks.
- You have had a blood clot or stroke (including mini-strokes or blood clots in the lungs or legs) within the past 6 months, with a specific exception for certain types of blood clots in the liver's portal vein (confirm with trial site).
- You currently have or have had a second type of cancer, unless it was an early-stage skin cancer or a very early cervical cancer that has been fully treated.
- You have HIV or another condition that weakens your immune system.
- You have taken part in another clinical trial using an experimental treatment within the past 30 days (or longer, depending on the previous treatment — confirm with trial site).
- You have certain other health conditions or complications, including: a history of serious lung inflammation, a combined hepatitis B and C infection, known inflammation of the pancreas, active tuberculosis, any active serious infection needing treatment, a history of organ or tissue transplant, a condition requiring immune-suppressing medication, an active autoimmune disease requiring treatment within the past 3 months (some exceptions apply — confirm with trial site), cancer spread to the brain (with some exceptions for those who have completed treatment and have no symptoms — confirm with trial site), or a live vaccine received within the past 30 days.
- You are currently taking any medication known to interfere with the drugs used in this trial.
- You are receiving any other cancer treatment not specified by this trial.
- You have taken any other experimental treatment within the past 28 days.
- You are pregnant, breastfeeding, or unwilling or unable to use a reliable form of birth control (specific acceptable methods are listed — confirm with trial site).
- You have a significant history of not following medical instructions or are unable to give informed consent reliably.
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: 86-21-64041990
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) evaluated by the investigator per Response Evaluation Criteria in Solid Tumors Version 1.1
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.