Researchers are looking for new ways to treat people with urothelial cancer (UC) that is locally advanced or metastatic. The standard treatment for locally advanced or metastatic UC is enfortumab vedotin (EV) given with pembrolizumab. The goals of this study are to learn about: * The safety of the study treatment when given with standard treatment and if people tolerate it * The number of people who have the cancer respond (cancer gets smaller or goes away) with the new study treatment when given with standard treatment.
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Number of Participants Who Experience an Adverse Event (AE)
Timeframe: Up to approximately 27 months
Number of Participants Who Experience a Dose Limiting Toxicity (DLT)
Timeframe: Up to approximately 21 days
Number of Participants Who Discontinue Study Treatment Due to an AE
Timeframe: Up to approximately 24 months
Objective Response Rate (ORR) as Assessed by Investigator
Timeframe: Up to approximately 58 months