Phase 3 Head and Neck Cancer Trial, Recruiting NCT07188584 Sponsor: Ming-Yuan Chen Condition: Head and Neck Cancer
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Phase 3 Head and Neck Cancer Trial, Recruiting

NCT07188584
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 aged between 18 and 70 years old.
  • People who have signed a consent form and are willing and able to attend appointments, follow the treatment schedule, and complete required tests as outlined in the study plan.
  • People newly diagnosed with cancer that has spread to distant parts of the body (metastatic), whose cancer showed a complete or partial response after receiving a standard first-line treatment of platinum-based chemotherapy combined with a PD-1 immunotherapy drug.
  • People diagnosed with a specific type of nasopharyngeal carcinoma (a cancer at the back of the nose/throat) — specifically the non-keratinizing type (WHO type II or III) — confirmed by tissue or cell testing, with visible spread shown on imaging scans.
  • People whose cancer is classified as stage IVB (the most advanced stage, meaning the cancer has spread to distant parts of the body) according to the AJCC 9th edition staging system.
  • People with a physical fitness score of 0 or 1 on the ECOG scale, meaning they are either fully active or have only mild limitations in physical activity (confirm with trial site).
  • Women who could become pregnant must have a negative pregnancy test (urine or blood) within 7 days before joining, and must agree to use effective contraception throughout the study.
  • Men whose partner could become pregnant must agree to use effective contraception throughout the study.

Who may not be able to join:

  • People who have fluid around the lungs that is related to cancer, or who have another type of cancer in addition to nasopharyngeal carcinoma.
  • People who have already received two or more rounds (lines) of systemic cancer treatment.
  • People with a known or suspected autoimmune disease, including conditions such as dementia or epilepsy.
  • People with moderate to severe heart conditions, including coronary heart disease, certain abnormal heart rhythms (including specific changes on a heart tracing test), or heart failure.
  • People who received steroid medications (glucocorticoids) — either throughout the body or in a specific area — within 4 weeks before joining the trial.
  • People who need to take immune-suppressing medications long-term, or who require steroids at doses high enough to suppress the immune system.
  • People who currently have active tuberculosis (TB), are being treated for TB, or who received TB treatment within the past year before screening.
  • People who are HIV positive; people who test positive for hepatitis B surface antigen with a detectable hepatitis B viral load above a certain level; or people who test positive for hepatitis C antibodies.
  • People who received any vaccine (such as a flu shot or chickenpox vaccine) within 4 weeks before joining the trial.
  • People whose treating doctor estimates their life expectancy to be less than 6 months at the time of joining the trial.
  • People who the treating doctor considers unsuitable for the trial for any other reason.

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 6 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

Phone: 86-13903052650

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
Ming-Yuan Chen
Registry
ClinicalTrials.gov
Start date
20 August 2025
Est. completion
1 December 2030

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2-year Progression-Free Survival (PFS); The incidence rate of radiotherapy-related ≥ grade 3 adverse events

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: 6 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