Zymfentra (Infliximab-dyyb) REal World Cohort STudy
Brief description of study
This study will enroll patients who are starting treatment with Zymfentra (infliximab-dyyb) for irritable bowel disease (IBD). This study will collect information about responses to Zymfentra in the “real world” setting. Zymfentra is approved by the United States Food and Drug Administration (FDA) for the treatment of IBD.
Clinical Study Identifier: s25-01094
Principal Investigator:
David P Hudesman.
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