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Trial ID IM101-240  |   NCT01357668

An Observational Registry of Abatacept in Patients With Juvenile Idiopathic Arthritis

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Sorry, this study is no longer accepting new participants, but is still ongoing.
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Summary

  • Male and Female Gender icon
  • 0-17
    Age Range
  • BMS Active Not Yet Recruiting Study icon
    Active, Not Recruiting

Overview

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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Key Eligibility Criteria

For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria

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

          Exclusion Criteria

          Exclusion Criteria Icon
          • Pregnant or nursing female at the time of enrollment
            1. Prior malignancies if the patient has not been malignancy free for at least 5 years.
              1. 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
                1. Known poor compliance with clinic visits (based on physician judgment).
                  Additional Information *

                  Treatment Options

                  Study Arms

                  ASSIGNED INTERVENTION

                  Study Arms

                  Patients with JIA who are treated with Abatacept

                  ASSIGNED INTERVENTION

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