drugset / Trial / NCT03053622

A Study of Mirikizumab (LY3074828) Injection in Healthy Participants

NCT03053622

Phase 1 Completed 67 enrolled Eli Lilly and Company
RandomizedParallel-groupOpen-labelBasic science

Summary

This study is conducted to compare how much mirikizumab, in two different formulations, is absorbed into the bloodstream and how long the body takes to get rid of it, when given as an injection under the skin or into the veins. Side effects of the injection will be collected. Each participant will be in the study for about 18 weeks, including screening.

Timeline

Start
2017-04-24
Primary completion
2018-04-03
Completion
2018-04-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirikizumab Monoclonal antibody 250 mg Subcutaneous

Indications

No indication recorded.