drugset / Trial / NCT03524092

A Maintenance Study of Mirikizumab in Participants With Moderately to Severely Active Ulcerative Colitis

NCT03524092

Phase 3 Completed 1328 enrolled Eli Lilly and Company
Non-randomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of mirikizumab as maintenance therapy in participants who completed as clinical responders in the prior 12-week induction study LUCENT-1 (NCT03518086).

Timeline

Start
2018-10-19
Primary completion
2021-11-03
Completion
2025-02-17

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Mirikizumab Monoclonal antibody 200 mg Subcutaneous
Subject Mirikizumab Monoclonal antibody 300 mg Subcutaneous

Indications