The purpose of this study is to evaluate the safety, tolerability, and drug levels of BMS-986454 in participants with Rheumatoid Arthritis
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Number of participants with adverse events (AEs)
Timeframe: Up to 6 months
Number of participants with serious adverse events (SAEs)
Timeframe: Up to 6 months
Number of participants with physical examination findings
Timeframe: Up to 6 months
Number of participants with vital sign measurement findings
Timeframe: Up to 6 months
Number of participants with 12-lead electrocardiogram (ECG) findings
Timeframe: Up to 6 months
Number of participants with clinical laboratory test findings
Timeframe: Up to 6 months
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