Phase 2 Head and Neck Cancer Trial, Recruiting NCT06851247 Sponsor: Sun Yat-sen University Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT06851247
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 who are willing to take part and sign a consent form in person.
  • People aged 18 to 65 years old, who are male or female and not pregnant.
  • People who have been diagnosed with a specific type of nasopharyngeal cancer (a cancer at the back of the nose/throat), confirmed by laboratory testing, classified as WHO type II or III (non-keratinising type).
  • People who have not yet received any cancer treatment and have no history of other cancers.
  • People whose cancer is classified as Stage IVa according to a specific international staging system (8th edition AJCC/UICC), meaning the cancer has spread to certain lymph nodes but not to distant parts of the body.
  • People who are generally well enough to carry out light activity and have no serious problems with the heart, lungs, liver, or kidneys (ECOG score of 0 or 1).
  • People whose blood test results meet minimum levels for red blood cells, white blood cells, and platelets (confirm with trial site for exact values).
  • People whose liver function tests are within acceptable ranges, specifically certain enzyme levels and bilirubin below set thresholds.
  • People whose kidney function is within an acceptable range, based on a blood test called serum creatinine.

Who may not be able to join:

  • People whose nasopharyngeal cancer has come back after treatment or has spread to distant parts of the body.
  • People whose cancer is of a different type called keratinising squamous cell carcinoma (WHO type I).
  • People who have received steroid medications (such as cortisone-type drugs) either throughout the body or to a specific area within the 4 weeks before joining the trial.
  • People who have taken part in another drug clinical trial within the 3 months before starting treatment.
  • People who have previously had an organ transplant or a stem cell transplant from another person.
  • People who have certain lung conditions, including a scarring lung disease, drug-related lung inflammation, a condition called bronchiolitis obliterans, radiation-related lung problems requiring treatment, active lung infection, or other moderate to severe lung diseases that significantly affect breathing.
  • People who have a condition that requires long-term use of medications that suppress the immune system.
  • People who have previously been treated with certain types of immunotherapy drugs (checkpoint inhibitors, including anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibodies) and whose cancer was found to be getting worse while on that treatment.
  • People who have an active autoimmune disease (where the immune system attacks the body) or a history of one — this includes conditions such as certain lung, eye, gut, liver, pituitary, kidney, or thyroid diseases; people with vitiligo (a skin pigmentation condition) or those whose childhood asthma fully resolved without ongoing treatment as adults may still be eligible, but people with asthma currently requiring medication generally may not be (confirm with trial site).
  • People who are HIV-positive, or who test positive for hepatitis B with a measurable level of the virus in their blood, or who test positive for both hepatitis C antibodies and active hepatitis C virus.
  • People who have received any vaccination against infections (such as flu or chickenpox vaccines) within the 4 weeks before joining the trial.
  • Women of childbearing age who test positive on a pregnancy test, or women who are breastfeeding.
  • People who would be unable to attend regular follow-up appointments due to personal, social, family, or geographic reasons.

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

Phone: 18820019088

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
3 January 2025
Est. completion
1 June 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2-year 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: 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