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:
- People aged 18 years or older
- People diagnosed with uveal melanoma (a type of eye cancer) that carries a high risk of spreading, defined by either the size or stage of the tumour (T2b, T2c, T2d, or T3 and above), or by specific abnormalities found on chromosomes 3 or 8 through a genetic test called CGH array
- People who finished treatment for their primary tumour no more than 2 months before joining the trial
- People who are able to attend scheduled visits and provide blood samples as required by the study
- People who have signed a consent form agreeing to take part (or whose legal representative has done so)
Who may not be able to join:
- People who do not have French social insurance (a form of national health coverage in France)
- People whose social, medical, or psychological situation would make it impossible to take part in the research process
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
Principal Investigator: Sophie Piperno-Neumann, MD, Institut Curie
Phone: 01 44 32 46 72
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
Description of the metastatic events and treatments in high risk UM patients and correlation to biomarkers; Biological study (lymphocytes); Biological study (ctDNA)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 13 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.