Phase 2 Head and Neck Cancer Trial, Recruiting NCT05628922 Sponsor: Fudan University Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT05628922
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:

  • You are willing to sign a consent form and are able to follow all the study requirements, including scheduled visits and tests
  • You were between 18 and 70 years old when diagnosed
  • You have been newly diagnosed with a specific type of nasopharyngeal cancer (a cancer at the back of the nose/throat), confirmed by a tissue sample, of the type called "non-keratinizing carcinoma"
  • Your cancer is at a locally advanced stage (meaning it has grown or spread to nearby lymph nodes but not to distant parts of the body), as classified by a standard cancer staging system
  • A blood test taken before treatment shows a detectable level of a virus marker called EBV DNA
  • You are generally in good physical health and able to carry out daily activities with little or no limitation (confirm with trial site)
  • You have not received any treatment for this cancer yet
  • Your blood counts are within a healthy range, including white blood cells, neutrophils, hemoglobin, and platelets
  • Your liver and kidney are functioning normally, based on blood test results
  • If you have hepatitis B, the virus level in your blood must be below a certain threshold at screening; if you have had hepatitis C, the virus must not be detectable at screening
  • If you or your partner could become pregnant, you must agree to use reliable contraception from the start of the study until one year after treatment ends

Who may not be able to join:

  • Your nasopharyngeal cancer is of a different tissue type, specifically "keratinizing carcinoma" or "basaloid squamous cell carcinoma"
  • You have had, or currently have, another type of cancer (with some exceptions such as certain treated skin cancers, cervical carcinoma in situ, or papillary thyroid cancer)
  • Your EBV DNA blood marker was undetectable before treatment
  • You have had radiation therapy in the past that could overlap with the area to be treated in this trial
  • You have already received surgery (other than a diagnostic biopsy), chemotherapy, immunotherapy, or biological therapy for this cancer
  • You are currently in another clinical trial involving a treatment intervention
  • You have taken high-dose steroid or immune-suppressing medications within the past 28 days
  • You have received a live vaccine within the past 30 days
  • You have had surgery or a significant injury within the past 30 days
  • You have serious or uncontrolled heart problems, such as heart failure, unstable chest pain, a heart attack within the past year, or certain heart rhythm problems
  • You have had a stroke within the past 6 months
  • You have had a serious active infection in the past 30 days that required treatment with antibiotics, antifungals, or antiviral medicines
  • You have an active autoimmune disease (a condition where the immune system attacks the body), with some exceptions such as controlled type 1 diabetes, thyroid conditions managed with hormone replacement, or stable vitiligo
  • You have tested positive for HIV, have another immune system disorder, or have had an organ transplant
  • You have had a lung inflammation condition (interstitial lung disease or pneumonitis) that required steroid treatment within the past year
  • You have active tuberculosis, or had tuberculosis within the past year, or had tuberculosis more than a year ago but did not complete standard treatment
  • Your hepatitis B or C virus levels are above the allowed thresholds in blood tests
  • You are pregnant or breastfeeding
  • You have any other serious condition, including mental health disorders, that the study doctor believes could put you at risk or make it difficult to participate safely

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 5 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: Chao-su Hu, M.D., Fudan University

Phone: +862164175590

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
Registry
ClinicalTrials.gov
Start date
2 July 2022
Est. completion
1 July 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-free survival

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: 5 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