Cure8 trial brief
Why This Matters
This registry will collect one-year, patient-reported outcomes on symptom control and clinical remission while people with IBD receive Zymfentra (infliximab-dyyb) in routine care — information that may help patients and clinicians understand real-world effectiveness of this infliximab biosimilar.
Who Should Pay Attention
Adult patients with Crohn's disease or ulcerative colitis, patients on biologics, clinicians prescribing infliximab/biosimilars, and IBD researchers.
Study Snapshot
What To Know
This is an observational (non-interventional) registry that aims to enroll about 200 participants who are prescribed Zymfentra during regular clinical care. Participants complete online surveys using the SCCAI and other timepoints up to 52 weeks; the study will describe symptom trajectories and remission rates as reported by patients.
The study is recruiting at multiple U.S. academic centers. Because it is observational, it tracks outcomes under usual-care conditions rather than assigning or randomizing treatments; it can provide useful real-world data but cannot prove causation or compare Zymfentra to other therapies in a randomized way.
Keep In Mind
This is an observational, non-randomized registry (recruiting) and will describe patient-reported outcomes over time; it does not establish causal efficacy compared with other treatments. The study record is a trial registration (ClinicalTrials.gov) describing planned data collection, not published trial results.
Source Details
Review the original publication for the complete reporting, methods, and context.
This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.