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Clinical Trial Summary

This registry is a multi-center, prospective, longitudinal, observational program that will gather and analyse data on participants treated with infliximab, golimumab, golimumab Intravenous (I.V) or ustekinumab. Treatment will be prescribed by the physician according to actual clinical practice or standard of care for Rheumatoid Arthritis (RA), Axial Spondyloarthritis (AxSpA) , Psoriatic Arthritis (PsA); there will be no randomized assignments to treatment. At baseline and approximately every 6 months thereafter, information will be collected to assess safety, clinical outcomes, quality of life, comorbidities, pharmacoeconomics and treatment regimens among cohorts of participants receiving infliximab, golimumab, golimumab I.V or ustekinumab for the treatment of RA, AxSpA and PsA.


Clinical Trial Description

Participants will be selected for this registry using a non-probability sampling method. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00741793
Study type Observational
Source Janssen Inc.
Contact
Status Completed
Phase
Start date February 12, 2002
Completion date June 29, 2018

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