Phase 2 Liver Cancer Trial, Recruiting NCT07123545 Sponsor: Zhejiang University Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT07123545
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 aged 18 to 75 years old
  • People who have been diagnosed with advanced liver cancer (hepatocellular carcinoma) confirmed by a tissue biopsy or sample
  • People whose cancer can be measured on a scan using standard medical criteria
  • People whose cancer has continued to grow or spread after at least 2 previous cancer treatments
  • People expected to live for at least 6 months
  • People who are generally well enough to carry out light activity and care for themselves (a doctor will assess this using a standard scale)
  • People who have tumor tissue available for detailed genetic testing, or who already have qualifying genetic test results on file
  • People whose blood counts, liver function, kidney function, and blood clotting results fall within the ranges required by the trial (a doctor will check these through blood tests)
  • Women who could become pregnant must have a negative pregnancy test within 7 days before starting treatment, and must agree to use highly effective contraception during the trial and for at least 120 days after the last treatment
  • Men must agree to use barrier contraception during the trial and for at least 120 days after the last treatment
  • People who are willing and able to attend all required visits, follow the study schedule, and complete all required tests and procedures

Who may not be able to join:

  • People who have had another active cancer in the past 5 years, unless it was a type of skin cancer that has been fully treated, early-stage cervical changes, or another cancer considered fully cured with very low chance of returning
  • People whose genetic testing does not find specific targets needed for the trial's treatment approach
  • People who have previously had a bone marrow, stem cell, or solid organ transplant from another person
  • People who have cancer that has spread to the brain or spinal fluid that is currently active or causing symptoms — previously treated and stable brain metastases may be considered in some cases (confirm with trial site), but spread to the lining of the brain or spinal cord is not permitted under any circumstances
  • People with an active bacterial, fungal, or mycobacterial infection that requires treatment, including untreated latent tuberculosis
  • People with certain active viral infections, including detectable hepatitis B virus, detectable hepatitis C virus, HIV, or active syphilis
  • People who have an active autoimmune disease that has required higher-dose immune-suppressing medication within the past 2 years — some conditions such as vitiligo, type 1 diabetes, stable thyroid conditions on medication, and mild psoriasis may still be considered (confirm with trial site)
  • People who have taken higher-dose immune-suppressing medication within 14 days before the planned treatment (low-dose topical, inhaled, or eye drop steroids are generally permitted)
  • People with serious uncontrolled heart conditions, uncontrolled high blood pressure, or significant lung disease
  • People with a history of substance use or a mental health or social situation that would make it difficult to give informed consent or follow the study requirements
  • People who have had a severe allergic reaction (grade 3 or higher) to a vaccine or similar investigational product, or who have any condition the trial doctor considers too risky for immunotherapy
  • People who have any other condition that, in the trial doctor's judgment, could affect their safety or the reliability of the trial results

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 22 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

Phone: +8619941463683

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
Zhejiang University
Registry
ClinicalTrials.gov
Start date
1 August 2025
Est. completion
31 July 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Successful Administration Rate of iNeo-Vac-T01; Incidence of Adverse Events (AEs)

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: 22 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