Phase 3 Head and Neck Cancer Trial, Recruiting NCT06258811 Sponsor: Lai-ping Zhong Condition: Head and Neck Cancer
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Phase 3 Head and Neck Cancer Trial, Recruiting

NCT06258811
Recruiting Phase 3

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 generally well enough to carry out daily activities with little to no limitation (measured by a standard medical scale called ECOG, scoring 0 or 1)
  • People who have been diagnosed with squamous cell carcinoma (a type of cancer) in the mouth, including the tongue, gums, cheek, floor of the mouth, hard palate, or the area near the back molars
  • People whose cancer is at stage III or IVA, based on specific tumour and lymph node measurements (AJCC 2018 staging system)
  • People who have at least one tumour that can be measured using standard imaging criteria (RECIST v1.1)
  • People whose blood cell counts fall within acceptable ranges — white blood cells, haemoglobin, and platelets must all be above certain levels
  • People whose liver function tests are within an acceptable range (ALT/AST and bilirubin levels below set thresholds)
  • People whose kidney function is within an acceptable range (based on a blood test called serum creatinine)
  • People whose blood clotting function is within an acceptable range (based on tests called INR, PT, and APTT)
  • People who have read and signed the trial's informed consent form

Who may not be able to join:

  • People who still have unresolved side effects (grade 2 or higher) from a previous cancer treatment
  • People with a known serious allergic reaction (grade 3–4) to any ingredient in the trial treatment
  • People with a known history of another cancer, unless it was fully treated and has not returned for at least 5 years
  • People who have previously had radiation therapy to the head or neck
  • People with a currently active and serious infection (above grade 2 on a standard medical scale)
  • People with significant heart problems — such as a recent heart attack, superior vena cava syndrome, or moderate-to-severe heart disease — diagnosed in the 3 months before joining the trial
  • People currently receiving any treatment that works through the immune system
  • People with a history of active bleeding, a blood clotting disorder, or who are taking a blood-thinning medication called coumarin (warfarin)
  • People who are pregnant or breastfeeding
  • People with active hepatitis B or hepatitis C, or other serious liver diseases such as autoimmune liver disease, primary biliary cirrhosis, sclerosing cholangitis, alcoholic liver disease, or non-alcoholic steatohepatitis (NASH)
  • People with a severe or uncontrolled infection, HIV infection, or a diagnosis of AIDS; or people with an uncontrolled autoimmune disease; or people who have had an organ, tissue, stem cell, bone marrow, or solid organ transplant
  • People who have participated in another clinical trial within 30 days before joining this trial
  • People whom the trial investigators consider unsuitable for participation for any other reason (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.

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 19 July 2026
Phase 3: approximately ~65% 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: Lai-ping Zhong, MD, PhD, Huashan Hospital

Phone: +862152888915

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 3
Sponsor
Lai-ping Zhong
Registry
ClinicalTrials.gov
Start date
20 February 2024
Est. completion
30 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Rate of 2-year event-free survival; Rate of 2-year overall 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: 19 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