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A 12-Week Open-Label Study to Investigate the Efficacy and Safety of Brepocitinib in Adults With Skin-Predominant Dermatomyositis

Dermatomyositis Clinical Trial

Official title:
A 12-Week Open-Label Pilot Study to Investigate the Efficacy and Safety of Oral Brepocitinib in Adults With Skin-Predominant Dermatomyositis

Clinical Trial Summary

This is a prospective, 12-week, open-label, single-arm study. The study population comprises individuals with refractory skin disease characteristic of dermatomyositis with no to minimal muscle involvement. After an up to 8-week Screening Period, eligible participants will receive brepocitinib 30 mg orally (PO) QD for 12 weeks.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06433999
Study type Interventional
Source Priovant Therapeutics, Inc.
Contact Lindsey Rios, BS
Phone (860) 307-5311
Email lindsey.rios@priovanttx.com
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date January 2025
View Details
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