Phase 2 Head and Neck Cancer Trial, Recruiting NCT07492914 Sponsor: West China Hospital Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT07492914
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:

  • Adults aged 18 or older, of any gender
  • People who have been diagnosed through laboratory testing with a type of head and neck cancer called squamous cell carcinoma (not including cancers of the nasopharynx, salivary glands, or thyroid), where a surgeon has assessed the tumour as removable or potentially removable
  • People whose general health and ability to carry out daily activities falls within an acceptable range, as measured by a standard medical scoring system (scores 0, 1, or 2 on the ECOG scale)
  • People whose blood counts, liver function, kidney function, and blood clotting results meet specific minimum levels set by the trial (confirm exact values with the trial site)
  • People who are willing to give written consent to participate and are able to attend scheduled visits and follow the trial procedures

Who may not be able to join:

  • People who have had another type of cancer in the past 5 years, unless it was fully treated and has not returned (certain low-risk skin cancers and early-stage cancers may be exceptions — confirm with trial site)
  • People who have an active autoimmune disease (where the immune system attacks the body) or a history of one, with the exception of type 1 diabetes that is stable on insulin
  • People who have a history of severe allergic reactions requiring hospitalisation, or who are known to be allergic to the types of medicines being used in this trial
  • People who have previously received certain types of immune checkpoint therapy (anti-PD-1, PD-L1, or anti-CTLA-4 medicines), a TROP2 antibody-drug treatment, or an anti-cancer vaccine
  • People who have received a live vaccine within the 4 weeks before the trial starts, or who plan to receive one during the trial; also people who have had major surgery or a serious injury within the 4 weeks before starting
  • People who have been taking medium-to-high dose steroid tablets or other medicines that suppress the immune system within the 14 days before starting (inhaled or skin-applied steroids and hormone replacement for adrenal conditions are generally permitted — confirm with trial site)
  • People with serious heart conditions, including certain types of heart failure, blocked heart arteries, significant heart rhythm problems, low heart pumping function, or an abnormal heart electrical reading
  • People with a known history of a lung scarring condition called interstitial lung disease, or active or uncontrolled tuberculosis
  • People with an overactive thyroid or other thyroid gland disease (people with an underactive thyroid that is stable on medication may still be considered — confirm with trial site)
  • People with an active infection, an unexplained fever in the 48 hours before starting, or who have been on antibiotic tablets or injections in the week before signing consent
  • People with active hepatitis B or C at certain levels of viral activity, a positive HIV test, or a history of AIDS
  • People with a confirmed diagnosis of a neurological or psychiatric condition such as epilepsy or dementia
  • People with a history of drug or alcohol misuse
  • People who are pregnant or breastfeeding; also people (or their partners) who are planning a pregnancy or who are not willing to use effective contraception during the trial and for 3 months after it ends
  • People who have taken part in another clinical drug trial within the 4 weeks before starting, or who are currently enrolled in another interventional trial
  • People whom the trial doctors consider unsuitable 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 26 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: +86-18384262516

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
Sponsor
West China Hospital
Registry
ClinicalTrials.gov
Start date
11 May 2026
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Major Pathological Response Rate (MPR)

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: 26 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