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Not Yet RecruitingNCT07446101

A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

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

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
450 (estimated)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGMirikizumabAdministered SC

Timeline

Start date
2026-03-01
Primary completion
2027-02-01
Completion
2027-02-01
First posted
2026-03-03
Last updated
2026-03-19

Locations

5 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07446101. Inclusion in this directory is not an endorsement.