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Clinical Trial Summary

The purpose of this study is to assess the effectiveness of Abatacept in real-world clinical practice. The main hypothesis to be examined in this study is, "Abatacept's effectiveness results in a single real-world clinic (n = 100) are reproducible at another site (n ~= 200)".


Clinical Trial Description

Two secondary hypotheses that will be tested are:

- Abatacept aids in achieving low disease activity or clinical remission in patients of the following Rheumatoid Arthritis (RA) sub-groups: RF+/CCP+, RF+/CCP- RF-/CCP+ RF-/CCP-; first time on a bio-tech drug; having previously failed a biological drug; having interstitial lung disease; identified as disabled; twenty-eight individual joints identified as {swollen, painful, tender, deformed or having decreased range of motion}; on or not on oral DMARD; age; or gender.

- A database with sufficient attributes exists from which a patient's efficacy on abatacept is accurately predictable. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01555879
Study type Observational
Source Arthritis Northwest PLLC
Contact
Status Completed
Phase N/A
Start date March 2012
Completion date November 2016

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