drugset / Trial / NCT06425549

A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Ustekinumab in Children and Adolescents From 6 Years to Less Than 18 Years of Age With Moderate to Severe Plaque Psoriasis

NCT06425549

Phase 3 Recruiting 168 enrolled UCB Biopharma SRL
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy of bimekizumab administered subcutaneously (sc) compared to active control (ustekinumab) in children and adolescents aged 6 to \<18 years of age with moderate to severe plaque psoriasis (PSO).

Timeline

Start
2024-06-25
Primary completion
2028-08-21
Completion
2030-11-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody Subcutaneous
Comparator Ustekinumab Monoclonal antibody Subcutaneous

Indications