Phase 2 Head and Neck Cancer Trial, Recruiting NCT07601737 Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT07601737
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 aged 18 to 75 years old
  • People who have been diagnosed with a specific type of cancer called squamous cell carcinoma in the head and neck area (such as the mouth, throat, voice box, or lower throat), at an advanced but not the most severe stage (Stage III to IVB)
  • People whose cancer has been assessed by a specialist team — including surgeons, radiologists, and pathologists — and considered suitable for surgical removal
  • People who are generally well enough to carry out light activity and care for themselves, with only minor limitations on physical activity (this is measured on a standard scale called ECOG, scores 0 or 1)
  • People with throat cancer in a specific location (oropharynx) who have had, or are able to have, a particular protein test called p16 carried out on their tumour
  • People who have tumour tissue available (either stored from a previous procedure or newly collected) for a protein test called PD-L1
  • People who have at least one tumour that can be measured on a scan
  • People with a life expectancy of at least 6 months
  • People whose blood counts, kidney function, and liver function fall within the acceptable ranges required by the trial (the trial site will check these through blood tests)
  • Women who are not pregnant and not breastfeeding, and who agree to use highly effective contraception during the trial and for 6 months after the last dose
  • Men who agree to use highly effective contraception during the trial and for 6 months after the last dose
  • People who are willing to give written consent and attend all required trial visits

Who may not be able to join:

  • People who have received certain cancer treatments — including PD-1 inhibitors, EGFR antibodies, EGFR-targeted therapies, or anti-blood-vessel growth drugs — within the 4 weeks before joining
  • People who have taken part in another interventional clinical trial within the past 30 days
  • People who, in the treating doctor's judgement, cannot safely receive platinum-based chemotherapy (cisplatin or carboplatin)
  • People whose cancer cannot be surgically removed, who are not medically well enough for surgery, who decline surgery for any reason, or whose tumour is too large to be removed
  • People who have had another cancer diagnosed within the past 5 years, except for a common and easily treated type of skin cancer called basal cell carcinoma
  • People with a history of a condition that causes the immune system to not work properly from birth or early life (primary immunodeficiency)
  • People with serious ongoing health conditions that are not well controlled, such as heart failure, severe lung disease, severe liver disease, or significant mental health conditions
  • People with a known HIV infection, active hepatitis B or C, or active tuberculosis
  • People who have had major surgery within the past 90 days, or who are planning major surgery unrelated to this cancer
  • People who have a known allergy or sensitivity to any of the drugs used in the trial
  • Women who are pregnant or breastfeeding, or people of childbearing potential who are unwilling or unable to use effective contraception during the trial and for at least 6 months after the last dose
  • People who, in the treating doctor's judgement, are not suitable for the trial for any other reason
  • People who are unwilling to participate or unable to give written consent
  • People who have received a live vaccine within 30 days before the first trial treatment

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 23 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+18616017916

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
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Registry
ClinicalTrials.gov
Start date
20 April 2026
Est. completion
30 April 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2-Year Event-Free Survival (EFS) Rate

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: 23 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