This multi-center observational study will evaluate the use of RoActemra/Actemra (tocilizumab) in monotherapy in patients with rheumatoid arthritis. Eligible patients initiated on RoActemra/Actemra treatment according to the licensed label will be followed for 6 months.

Read more: http://www.clinicaltrials.gov/ct2/show/NCT01643863?cond=%22Arthritis%22&lup_s=01/29/2014&lup_d=30