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Ulcerative Colitis

A Study of Mirikizumab (LY3074828) in Children and Teenagers With Ulcerative Colitis (UC)

AMBU | {{ defaultRegistry.registryAnchorText }} NCT04004611 {{ currentLocaleObject.registryAnchorText }}

Study Purpose

This study is designed to evaluate how the body processes and removes mirikizumab. The study will also evaluate safety and disease response in pediatric participants with UC taking mirikizumab.

Time Commitment

The study will last about 52 weeks and may include up to 17 visits.

Key Participation Requirements Tool Tip Icon

All clinical trials have rules about who can participate. This section outlines some of those rules. Please contact a study center to discuss the full set of criteria


Male Female


2 years
17 years

• Participants must weigh >10 kg • Participants must have a diagnosis of ulcerative colitis for at least 3 months before the planned start date for the study medications • Participants must have moderately to severely active UC as defined by a Modified Mayo Score (MMS) within 14 days before the first dose of study treatment • Participants must have evidence of UC extending proximal to the rectum • Participants must have demonstrated an inadequate response to, a loss of response to, or an intolerance to corticosteroids, immunomodulators, Janus kinase inhibitor (JAK-inhibitor) or to biologic therapies for UC • Participants must not have a current diagnosis of Crohn's disease, inflammatory bowel disease-unclassified (indeterminate colitis), ulcerative proctitis, or primary sclerosing cholangitis • Participants must not have had surgery to remove part of their colon • Participants must not have current evidence of toxic megacolon • Participants must not have received any of the following for treatment of UC: cyclosporine or thalidomide within 30 days of screening; corticosteroid enemas, corticosteroid suppositories, or topical treatment with 5-aminosalicyclic acid within 1 week of screening • Participants must not have inadequate response to Interleukin 12 p40 subunit antibody (anti-IL12p40) (e.g. ustekinumab) or had prior exposure to anti-IL-23p19 antibodies (e.g. risankizumab, brazikumab, guselkumab or tildrakizumab)

Where to Participate

Where to Participate

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