An Observational Registry of Abatacept in Patients With Juvenile Idiopathic Arthritis

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About the study

The purpose of this study is to examine the long-term safety of Abatacept for the treatment of juvenile idiopathic arthritis (JIA) with particular in interest in the occurrence of serious infections, autoimmune disorders, and malignancies.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

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  • Inclusion Criteria:

    1. Diagnosis of JIA (any subtype)
    2. Age < 18 years at the time of enrollment unless currently or previously enrolled in an abatacept clinical trial and received abatacept
    3. Receiving Abatacept at the time of enrollment as per treating physician's decision or received abatacept in a clinical trial
    4. Parent or legally acceptable representative willing to participate in the study and sign the informed consent

    EXCLUSION CRITERIA

    Exclusion Criteria:

    1. Pregnant or nursing female at the time of enrollment
    2. Prior malignancies if the patient has not been malignancy free for at least 5 years.
    3. Any serious acute or chronic medical condition other than JIA, including chronic infection, which would compromise the patient's ability to participate in the study
    4. Known poor compliance with clinic visits (based on physician judgment)
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    Study Locations

    Enter your ZIP code/Postal code/PIN code to locate study sites near you:

    How to Apply


    Contact the study center to learn if this study is a good match for you.

    Study’s details


    Contition
    Juvenile Idiopathic Arthritis
    Age (in years)
    < 17
    Participants needed
    800
    Est. Completion Date
    Jan 2, 2029
    Treatment type
    Observational

    Sponsor
    Bristol-Myers Squibb
    ClinicalTrials.gov identifier
    NCT01357668
    Study number
    IM101-240

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