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Zymfentra (Infliximab-dyyb) REal World Cohort STudy

NCT07237516

This study is recruiting at 11 US sites in 8 states, according to its ClinicalTrials.gov record last updated .

Summary

The goal of this observational study is to learn about how effective Zymfentra (IFX=dyyb) is when treating patients with Crohn's disease (CD) and ulcerative colitis (UC) Does Zymfentra lead to a reduction in symptoms at intervals throughout one year? Participants being prescribed Zymfentra (IFX-dyyb as part of their regular medical care for CD or UC will answer online survey questions about their bowel habits for 1 year.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Ulcerative Colitis (UC)
  • Crohn's Disease (CD)
  • Indeterminate Colitis
  • Inflammatory Bowel Disease (IBD)

Eligibility basics and study details

Study type
Observational
Phase
Not applicable
Ages
18 years and older
Sex
All
Healthy volunteers
Not accepted
Sponsor
University of North Carolina, Chapel Hill
Last updated on ClinicalTrials.gov
August 5, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Connecticut · 1

  • Yale University School of Medicine · New Haven, CT

Florida · 2

  • University of Miami · Miami, FL
  • AdventHealth · Orlando, FL

Iowa · 1

  • University of Iowa · Iowa City, IA

Maryland · 1

  • Mercy Medical Center · Baltimore, MD

Massachusetts · 1

  • Brigham and Women's Hospital · Boston, MA

New York · 1

  • New York University · New York, NY

North Carolina · 3

  • University of North Carolina · Chapel Hill, NC
  • Atrium Health Center for Gastroenterology and Surgery · Charlotte, NC
  • Wake Forest School of Medicine · Winston-Salem, NC

Ohio · 1

  • University of Cincinnati · Cincinnati, OH

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.