Trial Details

Not Recruiting
Basic Information
Clinical ID c5391
Identifier CTRI/2018/10/015908
Trial Title A Phase 3, Multicenter, Randomized, Double-Blind, Parallel, Placebo-Controlled Induction Study of Mirikizumab in Conventional-Failed and Biologic-Failed Patients with Moderately to Severely Active Ulcerative ColitisLUCENT 1
Trial URL Visit Original Page
Study Information
Study Results

NULL

Conditions Health Condition 1: K519- Ulcerative colitis, unspecified
Interventions Intervention1: blinded intravenous administration of300 mg mirikizumab: Patients will be randomized with 3:1 ratio to receive blinded Intravenous AdministrationDuration of treatment with the investigational product is 12 weeks.
Participant Information
Sponsor Eli Lilly and Company Lilly
City NULL
Country/Region Argentina;Australia;Austria;Belgium;Brazil;Canada;China;Croatia;Czech Republic;Denmark;France;Germany;Hungary;India;Ireland;Italy;Japan;Latvia;Lithuania;Malaysia;Mexico;Netherlands;Poland;Republic of Korea;Romania;Russia;Saudi Arabia;Serbia;Slovakia;Spain
Enrollment Criteria
Sex Requirement NOT SPECIFIED
Age Requirement NULL
Study Design
Study Type Interventional
Phase PHASE3
Time Information
Start Date NULL
Primary Completion Date NULL
Completion Date NULL