This 3 arm study will compare the safety and efficacy, with regard to reduction of signs and symptoms, of tocilizumab versus placebo, both in combination with methotrexate (MTX). in patients with moderate to severe active rheumatoid arthritis (RA) who currently have an inadequate response to MTX. Patients wil be randomized to receive tocilizumab 4mg/kg iv, tocilizumab 8mg/mg iv, or placebo iv, every 4 weeks; all patients will also receive methotrexate 10-25mg weekly. The anticipated time on study treatment is 3-12 months, and the target sample size is 500+ individuals.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
623
4mg/kg iv / month
8mg/kg iv / month
iv / month
10-25mg/week
Unnamed facility
Buenos Aires, Argentina
Unnamed facility
Buenos Aires, Argentina
Unnamed facility
Buenos Aires, Argentina
Unnamed facility
Adelaide, Australia
Unnamed facility
Douglas, Australia
Unnamed facility
Maroochydore, Australia
Percentage of patients with ACR 20 response
Time frame: Week 24
Percentage of patients ACR 50/70 responses; change from baseline in ACR core set components.
Time frame: Week 24
AEs, laboratory parameters, vital signs
Time frame: Throughout study
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Unnamed facility
Shenton Park, Australia
Unnamed facility
Vienna, Austria
Unnamed facility
Vienna, Austria
Unnamed facility
Vienna, Austria
...and 64 more locations