drugset / Trial / NCT02129777

Efficacy and Safety of Namilumab (MT203) for Plaque Psoriasis

NCT02129777

Phase 2 Completed 122 enrolled Takeda
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to establish proof of efficacy for namilumab in moderate to severe plaque psoriasis, measured as Psoriasis Area and Severity Index (PASI)75 response rate at Week 12.

Timeline

Start
2014-06
Primary completion
2015-09
Completion
2016-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Namilumab Monoclonal antibody 20 mg Subcutaneous
Subject Namilumab Monoclonal antibody 50 mg Subcutaneous
Subject Namilumab Monoclonal antibody 80 mg Subcutaneous
Subject Namilumab Monoclonal antibody 150 mg Subcutaneous

Indications