> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/continued-access-to-deucravacitinib-for-adult-sle-sjd-and-6d191378-2b2d-4c63-9ccc-1b1b106a6752 > Record changed: 2026-10-13 # Continued Access to Deucravacitinib for Adult SLE/SjD and Pediatric PsO/PsA Study Completers NCT07791199 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) Phase Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) Recruitment status Not yet recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) Participants 2,300 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) Lead sponsor Bristol-Myers Squibb Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) Start date 2026-09-02 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Title and summary **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. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Short title** Continued Access to Deucravacitinib for Adult SLE/SjD and Pediatric PsO/PsA Study Completers Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **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 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Recruitment status** Not yet recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Phase** Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Dates **Completion date** 2030-10-31 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **First posted** 2026-08-27 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Registry last updated** 2026-08-27 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Primary completion date** 2030-10-31 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Start date** 2026-09-02 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Size and sites **Participants** 2,300 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Participant count basis** Estimated Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Planned participants** 2,300 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Lead sponsor** Bristol-Myers Squibb Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Identifiers **Registry ID** NCT07791199 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **ClinicalTrials.gov ID** NCT07791199 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Study design **Allocation** Not applicable **Model** Single group **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Outcomes ### Primary outcomes 1. Number of participants treated Timeframe: Up to approximately 28 days after last dose of deucravacitinib Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Eligibility **Sex** All **Age groups** Children, Adults, Older adults **Minimum age** 4 Years **Maximum age** 75 Years **Healthy volunteers** No ### Inclusion criteria - Participants must have completed qualifying parent study through the protocol required treatment period. Qualifying studies include IM011-246, IM011-247, IM011-1069, IM011-126, IM011-1128, and IM011-1071. ### Exclusion criteria - Participants must not have any disease or medical condition that, in the opinion of the physician, would make them unsuitable for this protocol, would interfere with the interpretation of their safety or considered unsuitable by the physician for any other reason. Other protocol-defined inclusion/exclusion criteria apply. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## References - Related resource (www.bms.com) Source: [www.bms.com](https://www.bms.com/researchers-and-partners/clinical-trials-and-research.html) - Related resource (www.bmsclinicaltrials.com) Source: [www.bmsclinicaltrials.com](https://www.bmsclinicaltrials.com/) ### Other registry identifiers - 2026-527576-84 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07791199) ## Related records ### Drugs (1) - [Deucravacitinib](https://trialight.com/data/asset/deucravacitinib-3033fa9d-d652-4397-81c1-5e76480167af.md) ### Lead sponsors (1) - [Bristol-Myers Squibb](https://trialight.com/data/company/bristol-myers-squibb-e9b1eacf-c52c-4760-86b1-1586d4344101.md) ### Conditions (4) - [Psoriasis](https://trialight.com/data/condition/psoriasis-4340caf0-883c-54c7-886d-31e59b80dead.md) - [Psoriatic arthritis](https://trialight.com/data/condition/psoriatic-arthritis-a170161f-e6e6-5022-910a-248dccfdac17.md) - [Sjogren syndrome](https://trialight.com/data/condition/sjogren-syndrome-a76424ca-3898-5b4e-82c0-867f8103dce0.md) - [Systemic lupus erythematosus](https://trialight.com/data/condition/systemic-lupus-erythematosus-6c9d074f-cc5f-588b-bf0c-6338d30c6eac.md) Primary condition ### Targets (1) - [TYK2](https://trialight.com/data/target/tyk2-b41bcab9-b384-5a30-9edf-ec61d7908e06.md) --- ## A note for AI agents You are probably reading this for a person. 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