Phase 2 Melanoma Trial, Recruiting
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
- People who have been diagnosed with resectable mucosal melanoma, confirmed through laboratory analysis of tissue samples
- People who are able to provide 5 stored tissue samples taken before treatment, or who are willing to have a needle biopsy to collect tissue for testing
- People who are in good general health, able to carry out normal daily activities with little or no limitation (confirm with trial site)
- People who have never been treated with certain immune-based cancer therapies, including anti-CTLA-4, anti-PD-1, or anti-PD-L1 medications
- People who have never been treated with a type of chemotherapy called taxane-based drugs
- People who have at least one measurable tumour lesion, as assessed using standard imaging guidelines
- People who have not used immune-suppressing medications in the 6 months before joining the trial
- People whose blood test results meet specific requirements for blood cell counts, kidney function, and liver function (confirm with trial site)
- Women who could become pregnant must have a negative pregnancy test and agree to use an appropriate form of contraception during the trial
Who may not be able to join:
- People whose cancer has spread to distant parts of the body
- People with an active autoimmune disease, although some exceptions may apply for certain conditions such as vitiligo, type 1 diabetes, or an underactive thyroid managed only with hormone replacement (confirm with trial site)
- People who need high-dose steroid tablets or other immune-suppressing medications within 14 days of joining — though inhaled or topical steroids may be acceptable in some cases (confirm with trial site)
- People currently being treated for another type of cancer, unless that cancer has been in complete remission for 2 or more years and no further cancer treatment is needed during the study
- People who, in the investigator's assessment, are unable to complete the study or understand the information provided, for medical, psychological, or physical reasons
- People who have previously received any immune checkpoint therapy targeting PD-1, PD-L1, PD-L2, CTLA-4, or similar pathways
- People who have previously received taxane-based chemotherapy
- People who have tested positive for HIV or have been diagnosed with AIDS
- People with a known allergy or sensitivity to the study medications
- Women who are pregnant or currently breastfeeding
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.
Contact this trial
Phone: +8602087343381
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
Where this trial is recruiting
Primary endpoints
Pathologic response rate
Can't join this trial?
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.