This multi-center, observational study will evaluate the use in clinical practice and efficacy of RoActemra/Actemra (tocilizumab) in patients with rheumatoid arthritis. Eligible patients initiated on RoActemra/Actemra treatment according to the approved label will be followed for 6 months.
Study Type
OBSERVATIONAL
Enrollment
60
Unnamed facility
Athens, Greece
Unnamed facility
Athens, Greece
Unnamed facility
Athens, Greece
Unnamed facility
Larissa, Greece
Proportion of patients on RoActemra/Actemra treatment at 6 months
Time frame: approximately 2 years
Rates of dose modifications/interruptions
Time frame: approximately 2 years
Clinical/demographic patient characteristics at initiation of treatment
Time frame: approximately 2 years
Efficacy: Response according to total joint count evaluation by DAS28/EULAR/SDAI/CDAI/ACR
Time frame: approximately 2 years
Efficacy: Monotherapy versus combination therapy
Time frame: approximately 2 years
Use of disease-modifying anti-rheumatic drugs (DMARDs)
Time frame: approximately 2 years
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Unnamed facility
Pátrai, Greece
Unnamed facility
Pátrai, Greece
Unnamed facility
Rhodes, Greece
Unnamed facility
Thessaloniki, Greece
Unnamed facility
Thessaloniki, Greece