INSIGHT-IBD Pragmatic Study: Investigation of Mirikizumab in Real World Settings for Mirikizumab
Specialty Networks Research.
Summary
The goal of this study is to evaluate the real-world effectiveness of treatments for inflammatory bowel disease (IBD) within routine clinical practice. The study population includes adult patients (≥21 years) with ulcerative colitis (UC) or Crohn's disease (CD) receiving care in community gastroenterology practices in the United States. The main questions it aims to answer are: * Does treatment with mirikizumab reduce the proportion of patients requiring an increase in IBD disease management (e.g., unplanned visits, dose escalation, therapy switch, emergency department visits, or hospitalization)? * Does treatment with mirikizumab improve clinical outcomes, including disease activity, clinical remission, and patient-reported outcomes, compared to standard biologic therapy? * Researchers will compare patients treated with mirikizumab within the IBD Clinical Care Pathway versus patients receiving standard biologic therapies to see if mirikizumab leads to improved disease control and reduced healthcare utilization. Participants will: * Receive either mirikizumab or standard biologic therapy as part of routine clinical care * Attend follow-up visits at approximately 3, 6, 12, and 18 months * Have clinical data collected from electronic health records and healthcare utilization sources * Complete patient-reported outcome questionnaires assessing symptoms, quality of life, and daily functioning * Undergo routine laboratory tests and clinical assessments as part of standard care
Eligibility
- Age range
- 21+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Age ≥21 years at the time of enrollment * Confirmed diagnosis of ulcerative colitis (UC) or Crohn's disease (CD) * Eligible for treatment with biologic therapy for IBD, defined as failure of prior conventional therapy and/or prior biologic therapy (excluding IL-23p19 antagonists) * No prior exposure to mirikizumab and no contraindications to mirikizumab * Ability to provide informed consent * Willingness to comply with study procedures and follow-up requirements Exclusion Criteria: * Prior exposure to IL-23p19 antagonists (e.g., mirikizumab, risankizumab, guselkumab) *…
Interventions
- DrugMirikizumab
Mirikizumab administered according to approved dosing regimens for ulcerative colitis and Crohn's disease.
- DrugAnti-TNF agents
Biologic therapies administered per routine clinical care, including anti-TNF agents, anti-integrins, IL-12/23 antagonists, and IL-23p19 antagonists.
- Druganti-integrin antibodies
Biologic therapies administered per routine clinical care, including anti-TNF agents, anti-integrins, IL-12/23 antagonists, and IL-23p19 antagonists.
- DrugIL-12
Biologic therapies administered per routine clinical care, including anti-TNF agents, anti-integrins, IL-12/23 antagonists, and IL-23p19 antagonists.
- DrugIL-23
Biologic therapies administered per routine clinical care, including anti-TNF agents, anti-integrins, IL-12/23 antagonists, and IL-23p19 antagonists.
Locations (7)
- Arizona Digestive HealthSun City, Arizona
- GI Alliance of IllinoisGlenview, Illinois
- Gastroenterology Group of RochesterRochester, New York
- Texas Digestive Disease ConsultantsCedar Park, Texas
- Texas Digestive Disease ConsultantsFort Worth, Texas
- Digestive Health AssociatesHouston, Texas