This is a Phase I trial to evaluate the safety, tolerability and efficacy of nectin-4 targeting antibody-drug conjugate (SBE303) in participants with advanced solid tumors
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Incidence of adverse events and serious adverse events
Timeframe: Until trial completion (estimated 3 years)
Incidence of dose limiting toxicity
Timeframe: For the first cycle of treatment, through pre-dose Cycle 2 Day 1
Confirmed objective response rate
Timeframe: 32 weeks