drugset / Trial / NCT02529956

A Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of UCB4940 in Patients With Psoriasis

NCT02529956

Phase 1 Completed 39 enrolled UCB Celltech
RandomizedParallel-groupDouble-blindTreatment

Summary

To evaluate the safety of UCB4940 administered by iv infusion of a single ascending dose in subjects with mild to moderate plaque psoriasis.

Timeline

Start
2012-11
Primary completion
2014-01
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 8 mg Intravenous
Subject Bimekizumab Monoclonal antibody 40 mg Intravenous
Subject Bimekizumab Monoclonal antibody 160 mg Intravenous
Subject Bimekizumab Monoclonal antibody 480 mg Intravenous
Subject Bimekizumab Monoclonal antibody 640 mg Intravenous

Indications