drugset / Trial / NCT04137380

A Study of Mirikizumab in Healthy Chinese Participants

NCT04137380

Phase 1 Completed 60 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

The main purpose of this study is to evaluate the safety of the study drug known as mirikizumab. The study will investigate how the body processes the study drug. It will last up to about 4 months for each participant.

Timeline

Start
2019-12-04
Primary completion
2020-12-11
Completion
2020-12-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirikizumab Monoclonal antibody 200 mg Intravenous
Subject Mirikizumab Monoclonal antibody 300 mg Intravenous
Subject Mirikizumab Monoclonal antibody 400 mg Intravenous
Subject Mirikizumab Monoclonal antibody 600 mg Intravenous
Subject Mirikizumab Monoclonal antibody 1200 mg Intravenous

Indications

No indication recorded.