Phase 2 Head and Neck Cancer Trial, Recruiting NCT07457346 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT07457346
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 with a good general level of physical functioning, able to carry out normal daily activities with little or no limitation (as measured by a standard medical scale called ECOG 0–1).
  • People who have been confirmed by laboratory testing to have Stage III or Stage IVA squamous cell carcinoma (a specific type of cancer) in the head or neck area, including the mouth, throat, voice box, or surrounding structures.
  • People whose cancer falls into one of three groups: tumors that a surgical team considers removable upfront; tumors that may be removable but where surgery carries significant risks such as major disfigurement or loss of function (requiring specialist team discussion); or tumors that are too advanced for surgery due to involvement of critical nearby structures (confirm with trial site for exact grouping).
  • People whose blood test shows that a specific type of immune cell, called an exhausted T cell (identified by the markers PD-1, TIM-3, and CD8), makes up more than 10% of a certain group of immune cells in the blood.
  • People whose blood, kidney, and liver function results, taken within 14 days before joining, meet the required levels set by the trial (confirm specific values with trial site).
  • People who are able to understand the trial information, are willing to sign a consent form, and are able to attend all required appointments and follow-up visits.

Who may not be able to join:

  • People who have previously received certain types of immunotherapy drugs (such as anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 treatments) or a type of medication called JAK inhibitors, or who have had a severe allergic reaction to similar medications.
  • People who have an active autoimmune disease (where the immune system attacks the body) or who are currently taking steroid medications or other drugs that suppress the immune system.
  • People who have another active cancer, or an active infection such as tuberculosis, hepatitis, HIV, or related conditions that are not controlled.
  • People with serious heart or lung problems, bleeding or clotting disorders, a history of blood clot disease, or who are currently taking blood-thinning or clot-dissolving medications.
  • People who are pregnant or breastfeeding, or who are unwilling to use effective contraception throughout the trial period.

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 27 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: +8657187783521

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
1 January 2026
Est. completion
30 August 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathological Complete Response (pCR) Rate in Cohort A (Resectable); Objective Response Rate (ORR) in Cohort B (Potentially Resectable); Objective Response Rate (ORR) in Cohort C (Unresectable)

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: 27 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