Phase 3 Liver Cancer Trial, Recruiting NCT06644937 Sponsor: Zhujiang Hospital Condition: Liver Cancer
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Phase 3 Liver Cancer Trial, Recruiting

NCT06644937
Recruiting Phase 3

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 are willing to take part and have signed a consent form agreeing to participate in the study
  • Adults aged 18 to 75 years old (male or female)
  • People who have been diagnosed with hepatocellular carcinoma (a type of liver cancer) confirmed by tissue testing
  • People who had surgery to fully remove the liver tumour (called R0 resection) between 4 and 8 weeks before joining the trial, with no cancer left behind at the edges
  • People who have at least one of the following features that put them at higher risk of the cancer coming back after surgery: more than 3 tumours with at least one larger than 3 cm; a single tumour 5 cm or larger; signs of cancer cells found in blood vessels during or after surgery; cancer cells that look very abnormal under a microscope (low differentiation); the tumour capsule was invaded or had unclear borders; or the tumour had grown into nearby organs
  • People with a good general health and liver function, as measured by specific scoring systems used by doctors (ECOG score of 0–1 and Child-Pugh score of 5–6)
  • People who have not previously received any anti-cancer treatment for this liver cancer, except for up to 1–2 optional preventive procedures (TACE or HAIC) performed 4–8 weeks after surgery (confirm with trial site)

Who may not be able to join:

  • People whose liver cancer is a specific rare type, such as sarcomatoid hepatocellular carcinoma, mixed liver-bile duct cancer, or fibrolamellar hepatocellular carcinoma
  • People who have had another type of cancer in the past 5 years or are currently dealing with another cancer at the same time
  • People with serious problems affecting other major organs such as the heart, brain, lungs, or kidneys
  • People with a history of immune system problems or autoimmune diseases (conditions where the immune system attacks the body)
  • People who show signs that the cancer has already come back or spread before joining the trial
  • People who are known to be allergic to the study drug's ingredients, or who have had a severe allergic reaction to similar types of medicines (monoclonal antibodies or anti-angiogenic drugs)
  • People who have a history of hepatic encephalopathy (a condition where the liver is unable to remove toxins, affecting brain function)

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 13 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 15989187352

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

Status
Recruiting
Phase
Phase 3
Sponsor
Zhujiang Hospital
Registry
ClinicalTrials.gov
Start date
29 November 2024
Est. completion
31 October 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

1 year recurrence-free survival rate ,1-year RFSR.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov