This is a Phase 2/3, multi-arm, multi-stage, open-label study of human leukocyte antigen (HLA)-A\*02:01 negative participants with metastatic uveal melanoma (MUM) who will be randomized to receive either IDE196 + crizotinib or investigator's choice of treatment (pembrolizumab, ipilimumab + nivolumab, or dacarbazine).
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Phase 2a: To determine the optimal dose of IDE196 + Crizotinib combination for Phase 2B and Phase 3 by evaluating the following:
Timeframe: Approximately 5 months
Phase 2 Progression-Free Survival (PFS)
Timeframe: Approximately 2 years
Phase 3 Overall Survival (OS) of IDE196 + Crizotinib compared to investigator's choice of treatment.
Timeframe: Approximately 4 years