Phase 2 Head and Neck Cancer Trial, Recruiting NCT06811844 Sponsor: The First Affiliated Hospital of Xiamen University Condition: Head and Neck Cancer
Back to Head And Neck Cancer

Phase 2 Head and Neck Cancer Trial, Recruiting

NCT06811844
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 between 18 and 65 years old
  • People who have been diagnosed with nasopharyngeal carcinoma (a type of cancer in the back of the nose/throat) confirmed by a tissue or cell sample, at a specific stage of the disease (stage T1-4, N2-3, M0 — meaning it has spread to nearby lymph nodes but not to distant parts of the body)
  • People who have not previously had any cancer treatment, such as surgery, radiotherapy, or chemotherapy
  • People who have at least one tumour that can be measured on a scan, according to standard measurement guidelines
  • People who are generally well enough to carry out daily activities with little or no limitation (this is measured using a standard health scale called ECOG, scored 0 or 1)
  • People with an expected survival of at least 3 months
  • People who are willing and able to use contraception from the first dose of the trial medication until 24 weeks after the last dose (this applies to men and to women who could become pregnant)
  • People whose major organs (such as liver, kidneys, and blood system) are functioning within broadly normal ranges based on standard blood tests
  • People whose treating doctor believes the trial treatment is likely to offer a survival benefit

Who may not be able to join:

  • People with an active, known, or suspected condition where the immune system attacks the body (autoimmune disease)
  • People with high blood pressure that remains above a certain level (systolic above 160 mmHg or diastolic above 90 mmHg) even when taking blood pressure medication
  • People with a known inherited tendency to bleed or problems with blood clotting, or anyone who has had significant bleeding symptoms in the 12 weeks before screening, or who has lost more than 50 ml of blood within any 24-hour period
  • People with heart symptoms or heart conditions that are not well managed
  • People with certain lung conditions, including interstitial lung disease, medication-related lung inflammation, radiation-related lung inflammation requiring steroid treatment, currently active lung infection with symptoms, or severely reduced lung function
  • People with active hepatitis B or hepatitis C infection (based on specific virus level thresholds in blood tests)
  • People who are allergic to any of the medications used in this trial
  • People who are pregnant or breastfeeding
  • People who have any other condition or circumstance that the treating doctor believes could interfere with safe participation in the trial (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 14 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: 865922139531

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
The First Affiliated Hospital of Xiamen University
Registry
ClinicalTrials.gov
Start date
25 February 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response

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: 14 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