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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


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

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