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| Name | Class |
|---|---|
| National Data Bank for Rheumatic Diseases (NDB) | OTHER |
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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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Patients with rheumatoid arthritis initiating abatacept | |||
| Pts with RA initiating other biologic disease-modifying drugs | |||
| Pts w/ RA non-biologic disease-modifying anti-rheumatic drugs |
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| Measure | Description | Time Frame |
|---|---|---|
| Key safety outcomes (targeted infections, malignancies, mortality) | Every 6 months throughout the study |
| Measure | Description | Time Frame |
|---|---|---|
| Patient-reported infusion reactions | Every 6 months throughout the study | |
| Multiple sclerosis, lupus, and psoriasis | Every 6 months throughout the study | |
| Adverse events in pregnant women who receive abatacept |
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Inclusion Criteria:
Exclusion Criteria:
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Patients being treated for rheumatoid arthritis in the US
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| Name | Affiliation | Role |
|---|---|---|
| Bristol-Myers Squibb | Bristol-Myers Squibb | Study Director |
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| Label | URL |
|---|---|
| BMS Clinical Trial Information | View source |
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| ID | Term |
|---|---|
| D001172 | Arthritis, Rheumatoid |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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| Every 6 months throughout the study |
| Adverse events in subjects on abatacept who receive concomitant biologics | Every 6 months throughout the study |
| D003240 |
| Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D001327 | Autoimmune Diseases |
| D007154 | Immune System Diseases |