Head and Neck Cancer Trial, Recruiting
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:
For people with cancer:
- Adults aged 18 or older who have been diagnosed with Head and Neck Cancer and are planning to receive immunotherapy treatment
- People whose doctor has assessed their life expectancy to be at least 3 months
- People who have a tissue biopsy available, or existing tissue test results for certain cancer markers (called PD-L1 TPS and/or PD-L1 CPS), held at the participating hospital
For healthy participants (no cancer):
- Adults aged 18 or older who have never been diagnosed with any type of cancer
Who may not be able to join:
- People who have a diagnosed psychiatric (mental health) disorder
- People who have uncontrolled medical complications or other serious health conditions
- People who have difficulty with blood draws, or who are unwilling to attend scheduled follow-up blood collection appointments
- People whose doctor assesses them as unsuitable for participation in the study (confirm with trial site)
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.
Contact this trial
Principal Investigator: Hung-Ming Wang, Division of Oncology, Chang Gung Memorial Hospital
Phone: +886975368112
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
Where this trial is recruiting
Primary endpoints
ICI responses, concordance to tissue PD-L1 expression
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.