Liver Cancer Trial, Recruiting NCT06333561 Sponsor: Sun Yat-sen University Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT06333561
Recruiting Not Applicable

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 have been diagnosed with a specific type of liver cancer (called infiltrative hepatocellular carcinoma, or HCC) confirmed by MRI or CT scan
  • Your liver is functioning reasonably well, rated as Child-Pugh class A or B (confirm with trial site), and you are generally able to carry out daily activities with little or no limitation
  • Your first treatment for this condition is a drug called Lenvatinib
  • Depending on which group you are assigned to, you would receive either Lenvatinib alone, or a combination of Lenvatinib, a procedure called HAIC (a way of delivering chemotherapy directly to the liver), and an immunotherapy drug called a PD-1 inhibitor
  • You have no history of any other type of cancer
  • The cancer has not spread into the heart or the large vein connected to the heart (vena cava)

Who may not be able to join:

  • Your liver cancer has a defined outer layer or capsule surrounding the tumour
  • You are under 18 years old or over 75 years old
  • Your first treatment was a procedure called TACE (a different type of liver-directed therapy)
  • You previously received a drug called sorafenib or other systemic treatments, with or without an immunotherapy drug, after HAIC
  • Your medical imaging records are incomplete
  • You were lost to follow-up within the first three months after starting treatment

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 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Feng Duan, MD, Chinese PLA General Hospital

Phone: 86 19868000115

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
1 January 2021
Est. completion
30 December 2024

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall survival

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: 28 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