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A Study of Mirikizumab (LY3074828) in Pediatric Participants With Crohn's Disease

Recruiting · Phase 3 · NCT05509777

Conditions: Crohn's Disease

At a glance

Research payments reported, 2025
$200,969
U.S. investigators named
5
Sites paid
5
Planned or actual enrollment
90

About the trial

Sponsor
Eli Lilly and Company
Tested
Mirikizumab (drug)
Dates
Started 2024-03-13; completion 2028-04
Results posted
Not yet

Study participants will be screened during the platform study and randomly assigned to receive mirikizumab or another intervention. The purpose of the mirikizumab study is to evaluate efficacy, safety, tolerability, and how well mirikizumab absorbs into the body of pediatric participants with Crohn's disease. Study periods for the intervention-specific appendix (ISA) will be as follows: * A 12-week induction period * A maintenance period from Week 12 to Week 52, and * A safety follow-up period up to 16 weeks. The study will last about 74 weeks and may include up to 19 visits.

From ClinicalTrials.gov, last updated 2026-10-07. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Eli Lilly and Company reported $200,969 in research payments for this study in 2025 (5 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.