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Clinical Trials in the USA / NCT07446101
Recruiting Phase 1

A Study of Mirikizumab Solution (LY3074828) in Healthy Participants

NCT07446101 · tracked via the Priya Life Science USA tracker
Sponsor
Eli Lilly and Company
Phase
Phase 1
Started
2026-03-24
Last updated
2026-05-14

Condition(s) studied

Healthy

Investigational drug(s) / intervention(s)

Mirikizumab →

Mirikizumab: Administered SC

Study 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

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Are overtly healthy males or females as determined by medical evaluation including: * medical history * physical examination * clinical laboratory tests * ECG, and * vital signs. * Have clinical laboratory test results at screening and Day -1 within normal reference range. * Have a body mass index (BMI) within the range of 18.0 to 34.0 kilograms per square meter (kg/m²), inclusive. Exclusion Criteria: * Have significant allergies to humanized monoclonal antibodies or known allergies to mirikizumab, related compounds or any components of the formulation, or history of significant atopy. * Have significant previous or current history of comorbidities capable of significantly altering the absorption, metabolism, or elimination of drugs. * Have clinically significant multiple or severe drug allergies, or intolerance to topical corticosteroids, or severe post-treatment hypersensitivity reactions. * Are immunocompromised. * Intend to use over-the-counter or prescription medication, including herbal medications and traditional medications, within 7 days prior to dosing. * Have received treatment with biologic agents within 3 months or 5 half-lives, whichever is longer, prior to dosing. * Have previously received mirikizumab. * Have an abnormality in the 12-lead electrocardiogram (ECG). * Have clinically significant abnormalities in blood pressure, pulse rate, or body temperature. * Have a current or recent acute, active infection. * Have active tuberculosis (TB), or any history of active TB.

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
Fortrea Clinical Research Unit Daytona Beach Florida Recruiting
Axis Clinicals LLC Dilworth Minnesota Recruiting
Fortrea Clinical Research Unit Dallas Texas Recruiting
Worldwide Clinical Trials, Inc. San Antonio Texas Recruiting
Fortrea Clinical Research Unit Madison Wisconsin Recruiting

On this site

📄 Omvoh (mirikizumab) drug profile →

More Eli Lilly and Company trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07446101 on ClinicalTrials.gov ↗ ← All trials in the USA