This study will evaluate the clinical safety and efficacy of oral brepocitinib in participants with cutaneous sarcoidosis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
28
Drug: Oral Brepocitinib
Drug: Oral Placebo
Clinical Trial Site
San Francisco, California, United States
RECRUITINGClinical Trial Site
Durham, North Carolina, United States
RECRUITINGClinical Trial Site
Philadelphia, Pennsylvania, United States
RECRUITINGNumber of participants with Treatment Emergent Adverse Events and Serious Adverse Events as assessed by CTCAE v5.0
Time frame: Screening up to 28 days after the last dose of study drug at 16 weeks
Change from baseline in the Cutaneous Sarcoidosis Activity and Morphology Instrument Activity (CSAMI-A) score through Week 16.
CSAMI-A score is a measure of cutaneous sarcoidosis disease activity. A higher score indicates worse disease. Scores range from 0-165.
Time frame: 16 Weeks
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Clinical Trial Site
Madison, Wisconsin, United States
RECRUITING