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NOT YET RECRUITING
NCT07791199
PHASE3

Continued Access to Deucravacitinib for Adult SLE/SjD and Pediatric PsO/PsA Study Completers

Sponsor: Bristol-Myers Squibb

View on ClinicalTrials.gov

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

DRUG

Deucravacitinib

Specified dose on specified days