drugset / Trial / NCT01748539

A Phase 2 Clinical Study of KHK4827

NCT01748539 ↗

Phase 2 Completed 140 enrolled Kyowa Kirin, Inc.
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

EvaluationDrugModalityDoseRoute
Subject Brodalumab Monoclonal antibody 70 mg Subcutaneous
Subject Brodalumab Monoclonal antibody 140 mg Subcutaneous
Subject Brodalumab Monoclonal antibody 210 mg Subcutaneous

Indications