Stopped: Business objectives have changed
This is an extension study to evaluate safety and efficacy of ozanimod in participants with moderately to severely active Crohn's Disease.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Percentage of Participants With Clinical Remission
Timeframe: At weeks 48, 96, 144, 192, 240
Number of Participants With Treatment Emergent Adverse Events (TEAEs)
Timeframe: From first dose to 90 days post last dose (up to approximately an average of 19 months and a maximum of 65 months)