Phase 2 Liver Cancer Trial, Recruiting NCT06280105 Sponsor: Meng Chao Hepatobiliary Hospital of Fujian Medical University Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT06280105
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:

  • People who have signed a written consent form before enrolling
  • People aged over 18 years old, of any sex
  • People who have been diagnosed with intermediate or advanced liver cancer (hepatocellular carcinoma), confirmed by tissue or pathology testing, or people with liver scarring (cirrhosis) whose liver cancer has been diagnosed using recognised international clinical guidelines
  • People whose liver cancer has gotten worse while being treated with the combination of camrelizumab and apatinib
  • People whose liver is still functioning at a level called "Child-Pugh Class A" (confirm with trial site)
  • People with a general health and activity score of 0 or 1 on a standard medical scale (meaning they are fully active or have only minor limitations in physical activity)
  • People who have at least one tumour that can be measured using standard imaging guidelines
  • People whose doctors expect them to survive for at least 12 weeks
  • People whose blood counts, organ function, and other lab results meet specific minimum levels set by the trial (confirm with trial site for full details)
  • People with normal blood clotting results and no active bleeding or clotting conditions
  • Women who are not surgically sterilised and are of childbearing age must meet additional requirements (confirm with trial site)
  • People who are willing to participate fully and attend all required follow-up appointments

Who may not be able to join:

  • People whose liver cancer includes certain rare subtypes, such as fibrolamellar, sarcomatoid hepatocellular carcinoma, or bile duct cancer (cholangiocarcinoma), confirmed by testing
  • People who have a history of a condition called hepatic encephalopathy (brain problems caused by liver failure)
  • People who have previously had a liver transplant
  • People with significant fluid build-up around the heart, or fluid around the lungs that is causing symptoms and requires draining
  • People who have noticeable fluid build-up in the abdomen (ascites) that can be felt during a physical examination or needs to be drained
  • People who are infected with both hepatitis B (HBV) and hepatitis C (HCV) at the same time
  • People who have cancer that has spread to the brain or the lining around the brain or spinal cord
  • People who have had bleeding from swollen veins in the oesophagus or stomach within the 6 months before starting the trial
  • People who have had any significant bleeding event (grade 3 or above on a standard medical scale) within 4 weeks before starting the trial
  • People who have had a blood clot in an artery or vein within the 6 months before starting the trial
  • People with high blood pressure that is not controlled with medication
  • People with heart failure that is causing symptoms
  • People with serious bleeding tendencies or blood clotting disorders
  • People who have had a hole or abnormal opening in the gastrointestinal tract, or a bowel blockage, within the 6 months before starting the trial
  • People with an active autoimmune disease or a history of autoimmune disease (where the immune system attacks the body's own cells)
  • People who are living with HIV
  • People who, in the trial doctor's judgement, have other serious health conditions that could put them at risk or prevent them from completing the trial

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 20 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.

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Meng Chao Hepatobiliary Hospital of Fujian Medical University
Registry
ClinicalTrials.gov
Start date
31 March 2024
Est. completion
31 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

objective response rate (ORR) per RECIST1.1

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: 20 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