This observational study will evaluate the use and efficacy of RoActemra/Actemra (tocilizumab) in routine clinical practice in patients with moderate to severe rheumatoid arthritis. Eligible patients initiated on RoActemra/Actemra treatment in accordance with the local label will be followed for 6 months.
Read more: http://www.clinicaltrials.gov/ct2/show/NCT01741688?cond=%22Arthritis%22&lup_s=08/23/2013&lup_d=30
