Phase 2 Liver Cancer Trial, Recruiting NCT07337421 Sponsor: Northern Jiangsu People's Hospital Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT07337421
Recruiting Phase 2

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 between 18 and 75 years old
  • You have been diagnosed with liver cancer (hepatocellular carcinoma) confirmed by a tissue or cell sample, and you have not received any treatment for it before surgery (such as chemotherapy, targeted therapy, immunotherapy, radiation, or other procedures)
  • You had surgery to remove the liver cancer within the past 8 weeks, the surgeon removed all visible cancer with clear margins, and a scan taken at least 4 weeks after surgery confirmed no remaining signs of cancer
  • Your general health and ability to carry out daily activities is rated as fully active or restricted only in physically demanding activity (confirm with trial site)
  • You have at least one feature that puts you at higher risk of the cancer coming back, such as: a single tumor larger than 5 cm, cancer that has spread into nearby blood vessels, three or more tumors, an aggressive tumor type, or surgery margins of 1 cm or less
  • If your AFP blood marker (a liver cancer indicator) was high before surgery, it must have dropped significantly after surgery and not be rising again
  • If you have Hepatitis B or C, you must already be receiving standard antiviral treatment and be willing to continue it throughout the study
  • Your blood, liver, kidney, and clotting test results are within acceptable ranges as confirmed by your doctor
  • Your life expectancy is more than 12 months
  • You are not pregnant

Who may not be able to join:

  • Scans after surgery show that the cancer has spread outside the liver, or there are remaining or returning tumors
  • You have already received additional treatments such as chemoembolization (TACE) after your surgery
  • Your liver function is rated as grade B or C on the Child-Pugh scale, or you have a history of a condition called hepatic encephalopathy (brain problems caused by liver disease)
  • You have a significant fluid build-up around your heart, or you need fluid drained from around your lungs or abdomen
  • You have had a bleeding episode (such as from swollen veins in the food pipe or stomach) in the past 6 months, have untreated swollen veins considered high-risk for bleeding, or needed treatment for such veins in the past 28 days
  • You are unable to have contrast-enhanced CT or MRI scans of your liver
  • Your surgery did not fully meet the requirements for complete cancer removal
  • You have taken certain Chinese herbal medicines, traditional patent medicines, or immune-boosting drugs (such as thymosin or interferon) within the past 14 days
  • You have taken part in another drug clinical trial within the past 4 weeks
  • You have both Hepatitis B and active Hepatitis C at the same time
  • You have had a serious blood clot or cardiovascular event in the past 6 months, such as a heart attack, stroke, blood clot in the lungs, or deep vein thrombosis
  • You have significant heart or lung problems
  • You have a serious active infection, or had a severe infection (such as one requiring hospitalisation) within the past 4 weeks
  • You have a known allergy to any ingredient in the study drug, or a history of severe allergic reactions to traditional Chinese medicines
  • You have a known history of drug or alcohol misuse
  • You have a psychiatric condition that affects your ability to make decisions or give informed consent
  • You have any other serious health condition or abnormal test results that your doctor believes would make participation unsafe or unsuitable

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 23 July 2026
Phase 2: approximately ~30% 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

Principal Investigator: Dou-sheng Bai, Clinical Medical College, Yangzhou University

Phone: +86051487373382

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 2
Sponsor
Northern Jiangsu People's Hospital
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
1 September 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Recurrence-free survival (RFS)

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: 23 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