Long Term Experience With Abatacept in Routine Clinical Practice
NCT02109666 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2364
Last updated 2017-04-19
Summary
The purpose of this study is to estimate the retention rate of Abatacept over 24 months in routine clinical practice in every participating country depending on the treatment line.
Conditions
Interventions
- DRUG
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Bristol-Myers Squibb · Bristol-Myers Squibb
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-03-31
- Primary Completion
- 2016-02-29
- Completion
- 2016-02-29
Countries
- Austria
- Belgium
- Canada
- Czechia
- Denmark
- France
- Germany
- Greece
- Ireland
- Italy
- Netherlands
- Spain
- Switzerland
Study Locations
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