drugset / Trial / NCT00299546

A Study of the Safety and Efficacy of Golimumab (CNTO 148) in Subjects With Active Rheumatoid Arthritis Previously Treated With Biologic Anti-TNFa Agent(s)

NCT00299546 ↗

Phase 3 Completed 461 enrolled Centocor, Inc. Schering-Plough · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of golimumab (CNTO 148) in subjects who have active rheumatoid arthritis and have been treated previously with at least 1 dose of a biologic anti-TNFa agent (etanercept, adalimumab or infliximab).

Timeline

Start
2006-02
Primary completion
2007-08
Completion
2012-05

Outcome

Met primary endpoint

paper 28 (18%) patients on placebo, 54 (35%) patients on 50 mg golimumab (odds ratio 2.5 [95% CI 1.5-4.2], p=0.0006) PMID 19560810 ↗

registry analysis (superiority or other test); Group 1: Placebo vs Combined Golimumab; p <0.001; NCT00299546 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Golimumab Monoclonal antibody 50 mg Subcutaneous
Subject Golimumab Monoclonal antibody 100 mg Subcutaneous

Indications