drugset / Trial / NCT02129777
Efficacy and Safety of Namilumab (MT203) for Plaque Psoriasis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |