Rheumatoid Arthritis Clinical Trial
Official title:
Long Term Experience With Abatacept in Routine Clinical Practice
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.
Time Perspective: Other: Collection of the baseline data collected at Abatacept IV
initiation, prospectively or retrospectively within maximum 3 months following the first
administration. Other assessments are collected during the follow up period (maximum of 2
years by patient)
Biospecimen Retention: None Retained excepted for a local sub study (in Spain) where sample
with DNA was retained
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