The purpose of this study is to assess the safety and efficacy of tulisokibart in participants with moderately to severely active Ulcerative Colitis (UC). After the completion of the 12-week induction, all participants have the option to continue in the open-label extension for up to 170 weeks.
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Percentage of Participants in Cohort 1 Achieving Clinical Remission
Timeframe: Baseline and Week 12
Percentage of Participants Who Experienced an Adverse Event (AE)
Timeframe: Up to ~14 weeks
Percentage of Participants Who Discontinued Due to an AE
Timeframe: Up to ~14 weeks
Percentage of Participants Who Had One or More Serious Adverse Events
Timeframe: Up to ~14 weeks