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Active, Not Recruiting

Trial ID IM101-045B  |   NCT01088360

Safety Study of Abatacept to Treat Rheumatoid Arthritis (B)

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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
  • 18+
    Age Range
  • BMS Active Not Yet Recruiting Study icon
    Active, Not Recruiting

Overview

The purpose of this study is to compare the incidence rates of targeted infections, malignancies and mortality among patients with rheumatoid arthritis who are treated with abatacept and those who are treated with other anti-rheumatic medications.

Key Eligibility Criteria

Inclusion Criteria: - Signed informed consent - Diagnosis of rheumatoid arthritis - > 18 years at index treatment initiation or switch - Starting treatment with abatacept or new disease-modifying anti-rheumatic drug (including switching or adding) or biologic disease modifying drug. - Read/write English Exclusion Criteria: - None

Treatment Options

Study Arms

ASSIGNED INTERVENTION

Study Arms

Patients with rheumatoid arthritis initiating abatacept

ASSIGNED INTERVENTION

Study Arms

Pts w/ RA non-biologic disease-modifying anti-rheumatic drugs

ASSIGNED INTERVENTION

Study Arms

Pts with RA initiating other biologic disease-modifying drugs

ASSIGNED INTERVENTION

We strongly recommend you contact BMS to report Side Effects (Adverse Events)
Side Effects (Adverse Events) and other reportable events are defined here
Report Side Effects (Adverse Events) or Product Quality Complaints: Medical Information

Have questions? Live support is available 24/7 - Call 855-907-3286 or email clinical.trials@bms.com

Have questions? Live support is available 24/7 -
Call 855-907-3286 or email clinical.trials@bms.com