drugset / Trial / NCT06921850

A Study to Assess the Pharmacokinetics and Safety of Bimekizumab in Children and Adolescents With Moderate to Severe Hidradenitis Suppurativa

NCT06921850

Phase 3 Recruiting 40 enrolled UCB Biopharma SRL
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to assess the PK of bimekizumab following subcutaneous (sc) administration in study participants with moderate to severe hidradenitis suppurativa (HS)

Timeline

Start
2025-04-07
Primary completion
2026-12-21
Completion
2029-03-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody Subcutaneous