This study is designed to provide treatment with deucravacitinib for participants with SLE/SjD (Systemic Lupus Erythematosus/Sjögren's Disease) and pediatric participants with PsO/PsA (Psoriasis/Psoriatic Arthritis) who have completed their qualified parent studies and/or long-term extension if applicable.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2,300
Specified dose on specified days
Number of participants treated
Time frame: Up to approximately 28 days after last dose of deucravacitinib
BMS Clinical Trials Contact Center www.BMSClinicalTrials.com
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