drugset / Trial / NCT01474512

A Phase 3 Study in Participants With Moderate to Severe Psoriasis

NCT01474512 ↗

Phase 3 Completed 1296 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study will assess the safety and efficacy of LY2439821 compared to placebo in participants with moderate to severe, chronic plaque psoriasis.

Timeline

Start
2011-11-16
Primary completion
2014-06-24
Completion
2018-09-20

Outcome

Met primary endpoint

registry NUMBER Ixe Q4W: 76.4 percentage of participants NCT01474512 ↗

registry analysis (unspecified test); Placebo vs Ixe Q4W; p <0.001; Regression, Logistic NCT01474512 ↗

registry NUMBER Ixe Q4W: 82.6 percentage of participants NCT01474512 ↗

paper P<0.001 for all comparisons of ixekizumab with placebo PMID 27299809 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ixekizumab Monoclonal antibody 80 mg Subcutaneous

Indications