Head and Neck Cancer Trial, Recruiting NCT07618078 Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences Condition: Head and Neck Cancer
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Head and Neck Cancer Trial, Recruiting

NCT07618078
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 aged 18 to 75 years, of any gender
  • People who have been diagnosed with a specific type of nasopharyngeal cancer (cancer at the back of the nose/throat) confirmed by laboratory testing, and whose cancer tests positive for a marker called EBER
  • People whose cancer has not spread to distant parts of the body, confirmed to be at an early-to-intermediate stage using detailed scans and a standard cancer staging system
  • People who are generally well enough to carry out daily activities with little or no limitation (confirm with trial site for exact fitness level required)
  • People who have had a high-quality, contrast-enhanced MRI scan of the head and neck area before treatment, including specialised scan sequences, and who have at least one measurable area of cancer visible on imaging
  • People who have had a specific blood test measuring a virus-related marker (called cfEBV DNA) taken before treatment begins
  • People whose blood test results before treatment show healthy levels of red blood cells, white blood cells, and platelets, and whose liver and kidney function results are within an acceptable range, and who do not have severe hearing loss
  • People who are able to understand what the study involves and who have agreed in writing to take part, either personally or through a legally authorised representative
  • People who agree to allow the research team to use their clinical information, routine scan images, and leftover biological samples (such as blood samples and tissue slides) for research purposes
  • People whose major organs are functioning adequately, except for any effects directly caused by the nasopharyngeal cancer itself
  • People who are expected to reliably attend follow-up appointments over the long term and have consistent means of communication with the research team

Who may not be able to join:

  • People who did not have the cfEBV DNA blood test taken before treatment, or who are missing key information needed for a specific risk calculation used in this study (such as age, cancer stage, a particular enzyme level, or scan findings about the tumour)
  • People whose cancer has already spread to distant parts of the body (known as M1 or metastatic disease)
  • People who have had another type of cancer, unless it was a non-melanoma skin cancer or a very early cervical cancer that was fully treated and has shown no signs of returning for more than 5 years
  • People who are pregnant or breastfeeding, or people who are capable of having children and are unwilling to use effective contraception during the study period
  • People who are currently taking part in another clinical trial that involves an experimental drug or medical device
  • People who have serious or poorly controlled health conditions, which may include: a heart attack in the past 6 months, serious heart rhythm problems, a recent severe stroke, an active stomach or bowel ulcer, uncontrolled mental health conditions, uncontrolled diabetes, an active autoimmune disease, long-term use of medicines that suppress the immune system, a serious active infection requiring treatment, a known history of HIV, active hepatitis B with a high viral load, or hepatitis C with abnormal viral levels
  • People whose personal, social, geographic, or mental health circumstances would, in the trial team's judgment, make it impossible to attend regular follow-up visits and assessments

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
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: Junlin Yi, Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Phone: +86 18801342502

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
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Registry
ClinicalTrials.gov
Start date
1 January 2026
Est. completion
31 December 2031

Where this trial is recruiting

🇨🇳 China

Primary endpoints

3-year Failure-Free Survival (FFS)

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