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

Status Recruiting

Clinical Trial Summary

An Open-Label, Proof-Of-Concept, Study of Baricitinib for the Treatment of Pyoderma Gangrenosum

Clinical Trial Description

This is a Phase II study that will be open label and include a total of 20 patients who will receive the investigational product. PG will be defined by the investigator and a second reviewer on the basis of results from clinical, histological and laboratory assessments. These patients will undergo 24 weeks of baricitinib dosed daily and stable dose of prednisone dosed daily with follow-up until week 36. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04901325
Study type	Interventional
Source	Oregon Health and Science University
Contact	Alex G Ortega- Loayza, MD, MCR
Phone	503-418-3376
Email	ortegalo@ohsu.edu
Status	Recruiting
Phase	Phase 2
Start date	October 2023
Completion date	May 31, 2025

View Details

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