[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

855-907-3286

Email address

Clinical.Trials@bms.com

Condition

Juvenile Idiopathic Arthritis

Treatment type

Observational

Sponsor

Bristol-Myers Squibb

ClinicalTrials.gov identifier

NCT01357668

Study number

IM101-240

Understanding clinical trials

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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.

Who can take part?

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

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

  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)

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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