The purpose of this study is to assess the safety and tolerability of BMS-986525 alone and in combination with Nivolumab in participants with Relapsed/Refractory Small Cell Lung Cancer
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Number of participants with adverse events (AEs)
Timeframe: Up to approximately 2 years
Number of participants with serious adverse events (SAEs)
Timeframe: Up to approximately 2 years
Number of participants with AEs meeting dose-limiting toxicity (DLT) criteria
Timeframe: Up to 21 days
Number of participants with AEs leading to discontinuation
Timeframe: Up to approximately 2 years
Number of participants with AEs leading to death
Timeframe: Up to approximately 2 years
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