Phase 2 Liver Cancer Trial, Recruiting NCT05690048 Sponsor: Michael Dill Condition: Liver Cancer
Back to Liver Cancer

Phase 2 Liver Cancer Trial, Recruiting

NCT05690048
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 years or older
  • People who have been diagnosed with hepatocellular carcinoma (liver cancer), confirmed by imaging or tissue biopsy
  • People whose liver cancer cannot be treated with surgery, a liver transplant, or local treatments aimed directly at the tumour
  • People whose condition is considered appropriate for treatment with the medications Atezolizumab and Bevacizumab as part of standard care (confirm with trial site)
  • People who have at least one tumour that can be measured on scans, according to standard measurement guidelines called RECIST 1.1
  • People whose liver is still functioning reasonably well, as measured by a scoring system called Child-Pugh — specifically a score of A or B (with a maximum of 7 points)
  • People who are relatively physically well and able to carry out daily activities, as rated by a standard scale called ECOG performance status 0 or 1

Who may not be able to join:

  • People who have taken medications that suppress the immune system within the 6 months before starting the trial treatment
  • People who have, or have had, a condition where the immune system attacks the body (an autoimmune or inflammatory disorder)
  • People who have previously been treated with certain types of immune-based cancer therapies, including drugs that target CTLA-4, PD-1, PD-L1, or VEGF
  • People who have tested positive for HIV
  • People who have both hepatitis B and hepatitis C infections at the same time (note: people who previously had hepatitis C but no longer show the virus in their blood may still be eligible — confirm with trial site)
  • People who have been found on a recent scope examination (within the past 12 months) to have enlarged veins in the food pipe or stomach that the investigator considers at risk of bleeding
  • People who have ongoing nausea, vomiting, or a serious digestive condition, are unable to swallow tablets or capsules, or who have had significant bowel surgery that might affect how the body processes the study medication
  • People who have blood pressure that remains too high (above 150/90 mmHg) despite medical treatment, or who have had serious heart or blood vessel complications related to high blood pressure
  • People who have a history of serious kidney conditions involving protein leaking into the urine (nephrotic or nephritic syndrome)
  • People who have taken antibiotic medicines (taken by mouth or injection throughout the body) within 2 weeks before starting the trial treatment
  • People who have used probiotic products or supplements within 1 week before starting the trial treatment
  • People whose liver cancer is a specific less common type, including fibrolamellar, sarcomatoid, infiltrative-type, or a mixed liver and bile duct cancer
  • People who have had another separate primary cancer diagnosis
  • People who have received a live vaccine within 30 days before starting the trial treatment
  • People who are pregnant or breastfeeding
  • People who have had a serious allergic reaction to Atezolizumab, Bevacizumab, vancomycin, or any similar medications or their ingredients
  • People who are currently taking part in another interventional clinical trial
  • People who are detained in an institution by a legal or official order
  • People who do not have the legal capacity to consent for themselves
  • People with a known allergy to any component of vancomycin, atezolizumab, or bevacizumab

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 15 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: Michael T Dill, PhD, University Hospital Heidelberg, Heidelberg, Baden-Württemberg 69120

Phone: 06221 568611

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
Michael Dill
Registry
ClinicalTrials.gov
Start date
16 July 2025
Est. completion
1 March 2028

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Assessment of immunogenicity; Safety of the therapeutic combination in advanced HCC

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: 15 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