drugset / Trial / NCT04061395

Guselkumab for Hidradenitis Suppurativa, a Mode of Action Study.

NCT04061395

NaSingle-groupOpen-labelOther

Summary

This is a multicenter open-label mode of action study. Twenty patients with moderate to severe hidradenitis suppurativa will be treated with guselkumab 200 mg Q4W subcutaneously. Main objectie is to investigate changes in inflammatory pathways induced by IL-23p19 blockade with guselkumab, in HS lesional skin. The total duration of the treatment period per subject is 16 weeks.

Timeline

Start
2019-10-01
Primary completion
2021-12-30
Completion
2022-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Guselkumab Monoclonal antibody 200 mg Subcutaneous