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Males and females aged 4 to \\\u003C12 years for Cohort 2.\n* Plaque psoriasis for at least 6 months.\n* Moderate to severe disease.\n* Candidate for phototherapy or systemic therapy.\n* Must have completed the Week 52 treatment period in Part A or B for long-term extension (LTE) period.\n\nExclusion Criteria\n\n* Participants weighing ≤ 30.0 kg at screening for Cohort 1 (age 12 to \\\u003C 18 years), Part A and Part B. Participants weighing \\\u003C 18.0 kg at screening for Cohort 2 (age 4 to \\\u003C 12 years), Part A and Part B.\n* Other forms of psoriasis.\n* History of recent infection.\n* Prior exposure to deucravacitinib (BMS-986165) or another active comparator.\n* Evidence of active TB for LTE period.\n* Other protocol-defined inclusion\u002Fexclusion criteria apply.","ALL","4 Years","18 Years",{"count":812,"type":813},153,"ESTIMATED","INTERVENTIONAL",[816],"PHASE3","The purpose of this pediatric study is to evaluate the drug levels, efficacy and safety of Deucravacitinib in children and adolescent participants aged 4 to \\\u003C18 years with moderate to severe plaque psoriasis. This study includes two cohorts; Cohort 1 (age 12 to \\\u003C18 years) and Cohort 2 (age 4 to \\\u003C12 years), with two parts; for each cohort. Part A will evaluate the drug levels of BMS-986165 to enable selection of 2 dose levels to be studied in Part B. Part B will assess the efficacy and safety of two dose levels in children and adolescent participants with moderate to severe plaque psoriasis. The 5-year long-term extension (LTE) period will observe the long-term safety and tolerability of deucravacitinib in children and adolescent participants with psoriasis who have completed Parts A or B of the study.",[819],"Plaque Psoriasis",[821,822,823,25,824,825,819,826],"Adolescent Psoriasis","BMS-986165","Clinical trial","Children Psoriasis","Pediatric Psoriasis","Psoriasis","2026-06-05",{"date":829,"type":830},"2026-06-09","ACTUAL",{"date":832,"type":830},"2021-03-23",{"date":834,"type":813},"2033-09-08",{"name":5,"class":6},63]