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Trial ID IM011-1071  |   NCT06869551

A Study to Evaluate the Drug Levels, Efficacy, and Safety of Deucravacitinib (BMS-986165) in Pediatric Participants With Juvenile Psoriatic Arthritis

Summary

  • Phase 3
  • Male and Female Gender icon
  • 5-17
    Age Range
  • 21
    Locations
  • BMS Recruiting Study icon
    Recruiting

Overview

The purpose of this study is to evaluate the drug levels, efficacy, and safety of Deucravacitinib (BMS-986165) in pediatric participants with juvenile psoriatic arthritis.

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Key Eligibility Criteria

Inclusion Criteria

Inclusion Criteria Icon img
  • Participants must have been diagnosed with Juvenile Psoriatic Arthritis (JPsA).
    1. Participants must have at least three joints that are affected by arthritis.
      1. Participants must have tried at least one type of medicine for JPsA for at least three months, but it didn't work well or caused problems.

        Exclusion Criteria

        Exclusion Criteria Icon
        • Participants must not have been diagnosed with JPsA before 5 years of age.
          1. Participants must not have other types of Juvenile Idiopathic Arthritis (JIA) that aren't JPsA,
            1. Participants must not have a history of chronic eye inflammation (uveitis), or were diagnosed with uveitis within the last three months.
              Additional Information *
              • Other protocol-defined Inclusion/Exclusion criteria apply.

                Treatment Options

                Study Arms

                ASSIGNED INTERVENTION

                Study Arms

                Experimental: Arm A

                ASSIGNED INTERVENTION
                • Drug: Deucravacitinib

                Study Arms

                Placebo Comparator: Arm B

                ASSIGNED INTERVENTION
                • Drug: Deucravacitinib
                • Other: Placebo
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