drugset / Trial / NCT01101100

Study to Assess the Long-term Safety, Tolerability, and Efficacy of AMG 827 in Subjects With Psoriasis

NCT01101100

Phase 2 Terminated 181 enrolled Bausch Health Americas, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This study is an open-label extension of study 20090062 to evaluate extended subcutaneous dosing.

Timeline

Start
2010-04
Primary completion
2015-09
Completion
2015-09

Drugs

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

Indications