Liver Cancer Trial, Recruiting NCT04665388 Sponsor: University Health Network, Toronto Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT04665388
Recruiting Not Applicable

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 been diagnosed with a cancer linked to the Epstein-Barr virus (EBV), such as nasopharyngeal cancer (a type of cancer in the back of the nose and throat).
  • People who have been diagnosed with a cancer linked to the human papillomavirus (HPV), including certain squamous cell cancers of the head and neck, cervix, vulva, or anal canal. For head and neck cancers, a positive HPV test (or a related test called p16) is required; this is not required for cervical, vulvar, or anal canal cancers.
  • People with anal canal cancer where late-stage tumour tissue is preferred for the study, though early-stage tissue may be acceptable in some cases (confirm with trial site).
  • People with liver cancer (hepatocellular carcinoma, or HCC) who have above-normal levels of a protein called alpha-fetoprotein (AFP) in their blood, as measured by the hospital's standard reference range.
  • People who are 18 years of age or older.
  • People who have given their voluntary written agreement to take part in the trial.

Who may not be able to join:

  • People with any condition that, in the opinion of the trial doctor, could affect their safety during the study or make it difficult to properly analyse the samples collected.

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Kathy Han, MD, Princess Margaret Cancer Centre

Phone: 416-946-4501

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
30 November 2020
Est. completion
28 February 2027

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Identifying the p-HLA epitopes across diverse HLA alleles

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