drugset / Trial / NCT00810199

A Study of Tocilizumab and Methotrexate Treatment Strategies (Adding Tocilizumab to Methotrexate Versus Switching to Tocilizumab) in Patients With Active Rheumatoid Arthritis With Inadequate Response to Prior Methotrexate Treatment

NCT00810199 ↗

Phase 3 Completed 556 enrolled Hoffmann-La Roche
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This 2 arm study will compare 2 treatment strategies based on tocilizumab in combination with methotrexate or placebo in patients with moderate to severe rheumatoid arthritis. Patients receiving methotrexate treatment will be randomized to receive either a) tocilizumab 8 mg intravenous (iv) every 4 weeks + methotrexate orally (po) weekly or b) tocilizumab 8 mg iv every 4 weeks + placebo po weekly. After the first 24 weeks of blinded treatment, treatment adjustments (increase or decrease of treatment intensity) may be introduced at intervals, based on response. The anticipated time on study treatment is up to 3 years, and the target sample size is approximately 470 patients.

Timeline

Start
2009-03
Primary completion
2010-08
Completion
2013-01

Outcome

Missed primary endpoint

registry Tocilizumab + Methotrexate vs Tocilizumab + Placebo; p = 0.2055; Odds Ratio (OR) 1.260 (95% CI 0.882 to 1.799) NCT00810199 ↗

paper DAS28-ESR remission rates were 40.4% for TCZ+MTX and 34.8% for TCZ+PBO (p=0.19); PMID 22562983 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Methotrexate Small molecule 15 mg Oral
Subject Methotrexate Small molecule 17 mg Oral
Subject Tocilizumab Monoclonal antibody 8 mg/kg Intravenous

Indications