drugset / Trial / NCT00975130

Subcutaneous Golimumab (GLM) Plus DMARDs for Rheumatoid Arthritis, Followed by Intravenous/Subcutaneous GLM Strategy (P06129 AM2)

NCT00975130

Phase 3 Completed 3366 enrolled Merck Sharp & Dohme LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Part 1 of this trial will assess the safety and effectiveness of subcutaneous (SC) golimumab administered by autoinjector once monthly, when combined with different disease-modifying antirheumatic drug (DMARD) regimens used in daily rheumatology practice. Subsequently, Part 2 will study if a strategy of intravenous (IV) golimumab to induce remission followed by SC golimumab to retain remission is superior to continuing a SC regimen.

Timeline

Start
2009-09
Primary completion
2011-08
Completion
2012-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Golimumab Monoclonal antibody 2 mg/kg Subcutaneous
Subject Golimumab Monoclonal antibody 50 mg Subcutaneous

Indications