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Post-marketing Observational Study Assessing the Long-term Safety of Abatacept Using a Population-based Cohort of Rheumatoid Arthritis Patients in the Province of British Columbia


N/A
18 Years
N/A
Open (Enrolling)
Both
Rheumatoid Arthritis

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Trial Information

Post-marketing Observational Study Assessing the Long-term Safety of Abatacept Using a Population-based Cohort of Rheumatoid Arthritis Patients in the Province of British Columbia


Inclusion Criteria:



- Rheumatoid arthritis

- Receipt of abatacept, other biologic disease-modifying drug, or any non- biologic
disease-modifying anti-rheumatic drug

- Age 18 years or older

Exclusion Criteria:

- Below 18 years of age

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Serious infection

Outcome Time Frame:

Every 2 years throughout the study

Safety Issue:

Yes

Principal Investigator

Bristol-Myers Squibb

Investigator Role:

Study Director

Investigator Affiliation:

Bristol-Myers Squibb

Authority:

European Union: European Medicines Agency

Study ID:

IM101-213

NCT ID:

NCT01247766

Start Date:

December 2010

Completion Date:

August 2018

Related Keywords:

  • Rheumatoid Arthritis
  • Arthritis
  • Arthritis, Rheumatoid

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