RecruitingPhase 1NCT07446101

A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

An Adaptive Two-Stage Bioequivalence Study of Subcutaneous Injections of Mirikizumab Solution in Healthy Participants


Sponsor

Eli Lilly and Company

Enrollment

450 participants

Start Date

Mar 24, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The main purpose of this study is to assess the safety and tolerability of mirikizumab (LY3074828) solution formulation administered as a single injection compared with two injections under the skin in healthy participants. Blood tests will be performed to investigate how the body processes the study drug. For each participant, the study will last about 15 weeks.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Mirikizumab for people with healthy. The study is currently recruiting participants at 5 locations. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMirikizumab

Administered SC


Locations(5)

Fortrea Clinical Research Unit

Daytona Beach, Florida, United States

Axis Clinicals LLC

Dilworth, Minnesota, United States

Fortrea Clinical Research Unit

Dallas, Texas, United States

Worldwide Clinical Trials, Inc.

San Antonio, Texas, United States

Fortrea Clinical Research Unit

Madison, Wisconsin, United States

View Full Details on ClinicalTrials.gov

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NCT07446101


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