drugset / Trial / NCT00106535

A Study to Assess the Effect of Tocilizumab + Methotrexate on Prevention of Structural Joint Damage in Patients With Moderate to Severe Active Rheumatoid Arthritis (RA)

NCT00106535 ↗

Phase 3 Completed 1196 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This 3 arm study will compare the safety and efficacy, with respect to a reduction in signs and symptoms and prevention of joint damage, of tocilizumab versus placebo, both in combination with methotrexate (MTX) in patients with moderate to severe active rheumatoid arthritis. Patients will be randomized to receive tocilizumab 4 mg/kg IV, tocilizumab 8 mg/kg IV or placebo IV, every 4 weeks. All patients will also receive methotrexate, 10-25 mg/week. The anticipated time on study treatment is 1-2 years and the target sample size is 500+ individuals. After completion of the 2 year study participants could participate in the optional 3 year open label extension phase (year 3 to 5).

Timeline

Start
2005-01
Primary completion
2007-05
Completion
2012-07

Outcome

Met primary endpoint

registry analysis (superiority or other test); Placebo + Methotrexate vs Tocilizumab 4 mg/kg + Methotrexate; p <0.0001; Cochran-Mantel-Haenszel NCT00106535 ↗

registry analysis (superiority or other test); Placebo + Methotrexate vs Tocilizumab 8 mg/kg + Methotrexate; p <0.0001; Van Elteren's test NCT00106535 ↗

paper Compared with placebo-MTX, tocilizumab-MTX significantly inhibited structural joint damage and improved physical function in patients with RA PMID 23322466 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tocilizumab Monoclonal antibody 4 mg/kg Intravenous
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous
Background Methotrexate Small molecule 10 mg —
Background Methotrexate Small molecule 25 mg —

Indications