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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
5
Oral Brepocitinib PO QD
Clinical Trial Site
Scottsdale, Arizona, United States
The primary endpoint is the change in CDASI-A score from baseline through Week 12
Time frame: 12 weeks
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