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Continued Access to Deucravacitinib for Adult SLE/SjD and Pediatric PsO/PsA Study Completers
Sponsor: Bristol-Myers Squibb
Summary
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.
Official title: A Continuation Protocol for Deucravacitinib in Adult Patients With Systemic Lupus Erythematosus (SLE) or Sjögren's Disease (SjD) and Pediatric Patients With Psoriasis (PsO) or Psoriatic Arthritis (PsA) Who Have Completed Parent Studies
Key Details
Gender
All
Age Range
4 Years - 75 Years
Study Type
INTERVENTIONAL
Enrollment
2300
Start Date
2026-09-02
Completion Date
2030-10-31
Last Updated
2026-08-27
Healthy Volunteers
No
Interventions
Deucravacitinib
Specified dose on specified days