This multi-center, observational study will evaluate the clinical practice patterns, efficacy and safety of RoActemra/Actemra (tocilizumab) in patients with rheumatoid arthritis. Data will be collected from each eligible patient initiated on RoActemra/Actemra treatment by their treating physician according to approved label for up to 12 months from start of treatment.
Study Type
OBSERVATIONAL
Enrollment
51
Unnamed facility
Helsinki, Finland
Unnamed facility
Joensuu, Finland
Unnamed facility
Jyväskylä, Finland
Unnamed facility
Kuopio, Finland
Proportion of patients on RoActemra/Actemra treatment at 6 months
Time frame: approximately 2.5 years
Rates of dose modifications/interruptions
Time frame: approximately 2.5 years
Clinical/demographic patient characteristics at initiation of RoActemra/Actemra treatment
Time frame: approximately 2.5 years
Efficacy: Response according to joint count evaluation by DAS28/EULAR/SDAI/CDAI/ACR
Time frame: approximately 2.5 years
Efficacy: Monotherapy versus combination therapy
Time frame: approximately 2.5 years
Safety: Incidence of adverse events
Time frame: approximately 2.5 years
Quality of life: Patient global assessment of disease activity/VAS-Fatigue/VAS-Pain scales
Time frame: approximately 2.5 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
Lahti, Finland
Unnamed facility
Paimio, Finland
Unnamed facility
Riihimäki, Finland
Unnamed facility
Rovaniemi, Finland
Unnamed facility
Tampere, Finland
Unnamed facility
Vaasa, Finland