drugset / Trial / NCT01748539
A Phase 2 Clinical Study of KHK4827
RandomizedParallel-groupDouble-blindTreatment
Summary
This study is designed to evaluate the efficacy and safety of KHK4827 in subjects with moderate to severe plaque psoriasis in a randomized, double-blind, placebo-controlled, parallel group study. Pharmacokinetics of KHK4827 will also be assessed.
Timeline
- Start
- 2012-12
- Primary completion
- 2013-09
- Completion
- 2013-09
Outcome
Met primary endpoint
paper mean percentage improvements in the PASI scores were 37.7%, 82.2%, 96.8%, and 9.4% in the 70mg, 140mg, 210mg, and placebo groups, respectively, (p<0.001 PMID 26547109 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Brodalumab | Monoclonal antibody | 70 mg | Subcutaneous |
| Subject | Brodalumab | Monoclonal antibody | 140 mg | Subcutaneous |
| Subject | Brodalumab | Monoclonal antibody | 210 mg | Subcutaneous |