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A patient will be eligible for inclusion in this study if all of the following criteria apply:

  1. Uveal or cutaneous melanoma with MRD detected in molecular screening.
  2. Written (signed and dated) informed consent and be capable of co-operating with protocol
  3. Male or female, Age ³ 18 years.
  4. Life expectancy of at least 3 months.
  5. ECOG performance score of 0 or 1.
  6. No evidence of metastatic disease on a CT scan of neck/thorax/abdomen/pelvis for cohorts A and B and also on MRI liver for uveal melanoma for cohort B.
  7. Those receiving prior immunotherapy must have recovered from any immune-mediated adverse events (≤ grade 1) other than endocrinopathies on stable replacement therapy.
  8. Haematological and biochemical indices within the ranges shown in the trial protocol.

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