Phase 3 Liver Cancer Trial, Recruiting NCT07589244 Sponsor: Guangzhou Virotech Pharmaceutical Co., Ltd. Condition: Liver Cancer
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Phase 3 Liver Cancer Trial, Recruiting

NCT07589244
Recruiting Phase 3

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 willing to sign a consent form, understand what the study involves, and agree to follow all study procedures.
  • You are between 18 and 75 years old (inclusive) on the date you sign the consent form, regardless of gender.
  • You have been diagnosed with advanced liver cancer (hepatocellular carcinoma), either confirmed through a tissue or cell sample test, or diagnosed using recognised clinical guidelines.
  • Your general health and ability to carry out daily activities is rated as good or mostly good (a score of 0 or 1 on a standard doctor-used scale).
  • Your doctors expect you to live for at least 3 more months.
  • You do not have serious problems with your blood, liver, kidneys, blood clotting, or heart function.

Who may not be able to join:

  • You have previously been treated with certain specific medicines called camrelizumab or apatinib, or have received oncolytic virus therapy or other gene therapies.
  • You have taken another experimental drug or used an experimental medical device within the past 4 weeks (or within 5 half-lives of that drug, whichever is the shorter period), or your immune system is significantly weakened.
  • You have previously had your spleen removed.
  • You are currently pregnant or breastfeeding.

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 7 July 2026
Phase 3: approximately ~65% 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: Liang Peng, Third Affiliated Hospital, Sun Yat-Sen University

Phone: 020-85252621

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 3
Sponsor
Guangzhou Virotech Pharmaceutical Co., Ltd.
Registry
ClinicalTrials.gov
Start date
13 May 2026
Est. completion
31 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of Dose-Limiting Toxicities

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: 7 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