Actively Recruiting

Phase 1
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07446101

A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

Led by Eli Lilly and Company · Updated on 2026-05-14

450

Participants Needed

5

Research Sites

44 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be a healthy male or female as confirmed by medical history, physical exam, lab tests, ECG, and vital signs
  • Have normal lab test results at screening and the day before dosing
  • Have a body mass index between 18.0 and 34.0 kg/m2 inclusive
Not Eligible

You will not qualify if you...

  • Have significant allergies to humanized monoclonal antibodies, mirikizumab, related compounds, or components of the formulation, or a history of major atopy
  • Have serious past or current conditions that could affect drug absorption, metabolism, or elimination
  • Have severe drug allergies, intolerance to topical corticosteroids, or severe hypersensitivity reactions
  • Are immunocompromised
  • Plan to use any medications, including herbal or traditional medicines, within 7 days before dosing
  • Have received biologic agents within 3 months or 5 half-lives before dosing
  • Have previously been treated with mirikizumab
  • Have abnormal 12-lead ECG findings
  • Have significant abnormalities in blood pressure, pulse, or body temperature
  • Have a current or recent active infection
  • Have active tuberculosis or a history of active tuberculosis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Fortrea Clinical Research Unit

Daytona Beach, Florida, United States, 32117

Actively Recruiting

2

Axis Clinicals LLC

Dilworth, Minnesota, United States, 56529

Actively Recruiting

3

Fortrea Clinical Research Unit

Dallas, Texas, United States, 75247

Actively Recruiting

4

Worldwide Clinical Trials, Inc.

San Antonio, Texas, United States, 78217

Actively Recruiting

5

Fortrea Clinical Research Unit

Madison, Wisconsin, United States, 53704

Actively Recruiting

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Research Team

T

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or

CONTACT

P

Physicians interested in becoming principal investigators please contact

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

3

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