Liver Cancer Trial, Recruiting NCT06607120 Sponsor: Zhongda Hospital Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT06607120
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:

  • People who have been diagnosed with hepatocellular carcinoma (a type of liver cancer) confirmed by imaging scans, tissue sample, or cell testing
  • People whose liver cancer is classified as an advanced stage (BCLC Stage C), meaning the cancer has spread outside the liver and/or has grown into major blood vessels
  • People who have not previously received any systemic (whole-body) treatment for their liver cancer, such as chemotherapy, targeted therapy, or immunotherapy
  • People whose treatment included only commercially available (approved and marketed) checkpoint inhibitor drugs (PD-1/PD-L1 inhibitors) and anti-angiogenic drugs, though these do not need to be specifically approved for liver cancer
  • People who received a procedure called TACE (a treatment delivered directly to the liver's blood vessels) either after starting the above drug combination, or up to 3 months before starting it
  • People who received at least one full cycle of the combination drug therapy (PD-1/PD-L1 inhibitor plus anti-angiogenic drug) after the TACE procedure
  • People who have measurable liver tumours that can be tracked on repeated imaging

Who may not be able to join:

  • People whose liver cancer is a specific subtype, including cholangiocarcinoma, fibrolamellar, sarcomatoid hepatocellular carcinoma, or mixed hepatocellular/cholangiocarcinoma, as confirmed by tissue or pathology testing
  • People whose treatment history does not fit the required timing described in the inclusion criteria
  • People with severely reduced liver function (Child-Pugh Class C), a physical performance status score above 2, or severe brain complications related to liver disease (hepatic encephalopathy)

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: Gao- Teng, M.D, Zhongda hospital, Southeast university, Nanjing, China

Phone: +86-02583272121

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
Sponsor
Zhongda Hospital
Registry
ClinicalTrials.gov
Start date
1 June 2024
Est. completion
31 January 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Overall Survival(OS)

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