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A Nationwide Post-marketing Study on the Safety of Abatacept Treatment in Sweden Using the ARTIS Register


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

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Trial Information

A Nationwide Post-marketing Study on the Safety of Abatacept Treatment in Sweden Using the ARTIS Register


Inclusion Criteria:



- Resident of Sweden

Exclusion Criteria:

- None

Type of Study:

Observational

Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

Hospitalized infection

Outcome Time Frame:

Every 6 months 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:

IM101-125

NCT ID:

NCT01094795

Start Date:

July 2008

Completion Date:

October 2017

Related Keywords:

  • Rheumatoid Arthritis
  • Arthritis
  • Arthritis, Rheumatoid

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