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A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

NCT07446101

This study is recruiting at 5 US sites in 4 states, according to its ClinicalTrials.gov record last updated .

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.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Healthy

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 to 65 years
Sex
All
Healthy volunteers
Accepted
Sponsor
Eli Lilly and Company
Last updated on ClinicalTrials.gov
May 14, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Florida · 1

  • Fortrea Clinical Research Unit · Daytona Beach, FL

Minnesota · 1

  • Axis Clinicals LLC · Dilworth, MN

Texas · 2

  • Fortrea Clinical Research Unit · Dallas, TX
  • Worldwide Clinical Trials, Inc. · San Antonio, TX

Wisconsin · 1

  • Fortrea Clinical Research Unit · Madison, WI

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.