drugset / Trial / NCT03707717

A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer Participants

NCT03707717

Phase 1 Completed 189 enrolled UCB Biopharma S.P.R.L.
RandomizedParallel-groupOpen-labelBasic science

Summary

The purpose of the study is to evaluate the pharmakokinetics (PK), safety, tolerability, and immunogenicity of bimekizumab (BKZ) when administered subcutaneously (sc) via 3 different BKZ delivery devices in healthy participants.

Timeline

Start
2018-10-15
Primary completion
2019-06-05
Completion
2019-06-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.