drugset / Trial / NCT03766685

A Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or the Auto-injector for the Subcutaneous Self-injection of Bimekizumab Solution by Subjects With Moderate to Severe Chronic Plaque Psoriasis (PSO)

NCT03766685 ↗

Phase 3 Completed 172 enrolled UCB Biopharma SRL
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the ability of subjects with moderate to severe chronic plaque psoriasis (PSO) to safely and effectively self-inject bimekizumab at study start and 8 weeks after training in self-injection technique using a prefilled safety syringe or an auto-injector.

Timeline

Start
2018-12-20
Primary completion
2020-07-14
Completion
2020-09-08

Outcome

Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)

paper The ability of patients to safely and effectively self-inject bimekizumab was assessed at 8 weeks (primary endpoint) PMID 35133113 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Bimekizumab Monoclonal antibody 320 mg Subcutaneous

Indications