Guselkumab in the Treatment of Adults With Pyoderma Gangrenosum (PG)

Participation Deadline: 08/13/2027
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Description

This is a Phase II study that will be open label and include a total of 17 patients who will receive the investigational product. PG will be defined by the investigator on the basis of results from clinical, histological and laboratory assessments. These patients will undergo 28 weeks of guselkumab dosed every 4 weeks and a stable dose of prednisone dosed daily with follow-up until week 40.