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NCT06696014Terminated

Mirikizumab Real World Protocol

MIrikizumab in UC - a Real-woRld prOspective multicenteR Registry

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

The goal of this observational study is to learn about how effective mirikizumab (Omvoh) is when treating patients with ulcerative colitis (UC) Does mirikizumab (Omvoh) lead to a reduction in symptoms at intervals throughout one year? Participants being prescribed mirikizumab (Omvoh) as part of their regular medical care for UC will answer online survey questions about their bowel habits for 1 year.

Status (registry)
Terminated
Study type
Observational
Enrollment
6 (actual)
First submitted
11 Nov 2024
Start date
8 May 2025
Primary completion date
8 Jul 2026
Lead sponsor
University of North Carolina, Chapel Hill
NCT number
NCT06696014

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients will be excluded if they meet any of the following criteria:
  • Inability to provide informed consent.
  • Non-English speaking.
  • Patients presenting for a one-time consultation.

Who the study is looking for

  • Adult patients, age 18 years or older, with UC, who within 2 weeks have been started on mirikizumab therapy for moderate to severe UC or who plan to begin this therapy within the next 2 weeks. The start of the mirikizumab treatment must have been or be initiated in the setting of standard-of-care therapy.
  • Anticipation that the patient will be followed by the participating center for the next 12 months.
  • Diagnosis of UC must be established based on standard clinical, radiographic, endoscopic, and histologic criteria as described below.
    • Criteria for diagnosis of UC The following diagnostic criteria were developed by the NIDDK IBD Genetics Consortium and are provided as guidelines to complete documentation on individuals with Ulcerative Colitis.
  • Symptoms including one or more: diarrhea, rectal bleeding, abdominal pain, fever, extraintestinal manifestations, weight loss, or failure to thrive.
    • AND
  • Symptoms on two or more occasions separated by at least 8 weeks or ongoing symptoms of at least 6 weeks duration.
    • AND
  • Endoscopic Findings compatible with UC:
  • Superficial inflammation and/or ulceration (involving only the mucosa and submucosa) of the colon, which is continuous from the rectum extending proximally without skip lesions or complete rectal sparing (relative rectal sparing is allowed for patients receiving topical, rectal therapy; patchiness of endoscopic inflammation may be observed in patients with partially treated ulcerative colitis).
  • In patients with proctitis or left-sided ulcerative colitis, there may be an area of inflammation in the cecum, usually surrounding the appendiceal orifice.
  • No inflammation of the small intestine ("backwash ileitis" is allowed - non-stenotic superficial inflammation of the terminal ileal mucosa associated with severe pancolitis, which resolves following medical or surgical treatment of the colitis).
  • No features of Crohn's disease listed above. There is no minimum length of extension of UC required for inclusion in this study.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
TIDHI Innovation Inc.
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
University of North Carolina
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status
Medical University of South Carolina (MUSC)
Coordinator of this site? Confirm its status
CharlestonUnited StatesUnknown status
South Denver Gastroenterology
Coordinator of this site? Confirm its status
DenverUnited StatesUnknown status
University of Iowa Health Care
Coordinator of this site? Confirm its status
Iowa CityUnited StatesUnknown status
University of Louisville, Clinical Trials Unit
Coordinator of this site? Confirm its status
LouisvilleUnited StatesUnknown status
AdventHealth
Coordinator of this site? Confirm its status
OrlandoUnited StatesUnknown status
University of Rochester Medical Center
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status
Southern Star Research Institute, LLC
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.