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Clinical Trial Summary

The purpose of this study is to assess Abatacept Intravenous (IV) effectiveness in patients with inadequate response to one or more conventional Disease Modifying Against Rheumatism (DMARDs) including Methotrexate in France, through the estimation of Abatacept retention rate over 2 years and reasons of discontinuation


Clinical Trial Description

Observational Model:

Other: ReACTION is a study using secondary data originally collected in ACTION study. In ACTION, data were collected prospectively from October 2010 up to 2015 at each clinical visit. In France, data collection started in June 2011 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02037737
Study type Observational
Source Bristol-Myers Squibb
Contact
Status Completed
Phase N/A
Start date September 30, 2016
Completion date January 31, 2018

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