Safety Study of Abatacept to Treat Rheumatoid Arthritis
NCT ID: NCT01247766
Last Updated: 2025-03-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
6367 participants
OBSERVATIONAL
2010-12-31
2014-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with rheumatoid arthritis (RA) who receive abatacept
No interventions assigned to this group
Patients with RA who receive BDM drugs
biologic disease-modifying (BDM)
No interventions assigned to this group
Patients with RA who receive non-biologic DMARDs
disease-modifying anti-rheumatic drugs (DMARDs)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Receipt of abatacept, other biologic disease-modifying drug, or any non- biologic disease-modifying anti-rheumatic drug
* Age 18 years or older
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Arthritis Research Centre of Canada
OTHER
Bristol-Myers Squibb
INDUSTRY
Responsible Party
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Principal Investigators
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Bristol-Myers Squibb
Role: STUDY_DIRECTOR
Bristol-Myers Squibb
Related Links
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BMS Clinical Trial Information
Investigator Inquiry Form
FDA Safety Alerts and Recalls
Other Identifiers
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IM101-213
Identifier Type: -
Identifier Source: org_study_id
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