drugset / Trial / NCT00361335

A Study of Safety and Effectiveness of Golimumab in Participants With Active Rheumatoid Arthritis Despite Methotrexate Therapy

NCT00361335 ↗

Phase 3 Completed 643 enrolled Centocor, Inc. Schering-Plough · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the clinical effectiveness and safety of golimumab intravenous (IV) infusions every 12 weeks with or without Methotrexate (MTX), compared with MTX alone, in patients with active rheumatoid arthritis (RA) despite concurrent MTX treatment. In addition, the safety of subcutaneous (SC) golimumab injections following transition from IV golimumab infusions will also be evaluated.

Timeline

Start
2006-09
Primary completion
2007-12
Completion
2009-09

Outcome

Missed primary endpoint

paper The primary study end point was not met. PMID 20131276 ↗

registry Group V: IV Placebo + MTX vs Group VI: Combined Groups I and III; p = 0.051; 2-sided Cochran-Mantel-Haenszel NCT00361335 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Golimumab Monoclonal antibody 2 mg/kg Intravenous
Subject Golimumab Monoclonal antibody 4 mg/kg Intravenous
Subject Golimumab Monoclonal antibody 50 mg Intravenous
Subject Methotrexate Small molecule — —

Indications