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Trial ID IM101-240  |   NCT01357668

An Observational Registry of Abatacept in Patients With Juvenile Idiopathic Arthritis

Summary

  • Male and Female Gender icon
  • 0-17
    Age Range
  • 63
    Locations
  • BMS Recruiting Study icon
    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: - Diagnosis of JIA (any subtype) - Age < 18 years at the time of enrollment unless currently or previously enrolled in an abatacept clinical trial and received abatacept - Receiving Abatacept at the time of enrollment as per treating physician's decision or received abatacept in a clinical trial - Parent or legally acceptable representative willing to participate in the study and sign the informed consent Exclusion Criteria: - Pregnant or nursing female at the time of enrollment - Prior malignancies if the patient has not been malignancy free for at least 5 years. - 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 - Known poor compliance with clinic visits (based on physician judgment)

Treatment Options

Study Arms

ASSIGNED INTERVENTION

Study Arms

Patients with JIA who are treated with Abatacept

ASSIGNED INTERVENTION
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