drugset / Trial / NCT02568423

A Study of Mirikizumab (LY3074828) in Healthy Participants

NCT02568423

Phase 1 Completed 51 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study is to explore the safety and tolerability of mirikizumab in healthy Japanese and Caucasian participants. The study will also estimate how much mirikizumab gets into the blood stream and how long it takes the body to remove it. The study is expected to last about 16 weeks for each participant.

Timeline

Start
2015-12-02
Primary completion
2018-07-16
Completion
2018-10-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirikizumab Monoclonal antibody 60 mg Intravenous
Subject Mirikizumab Monoclonal antibody 200 mg Intravenous
Subject Mirikizumab Monoclonal antibody 600 mg Intravenous
Subject Mirikizumab Monoclonal antibody 1200 mg Intravenous
Subject Mirikizumab Monoclonal antibody 2400 mg Intravenous

Indications

No indication recorded.