drugset / Trial / NCT02141997

A Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexate in Subjects With Active Rheumatoid Arthritis Who Have an Inadequate Response to Methotrexate

NCT02141997

Phase 2 Completed 222 enrolled AbbVie
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a Phase 2 randomized, double-blind, double-dummy, parallel-group study designed to assess the safety, tolerability, efficacy, pharmacokinetics and immunogenicity of multiple doses of ABT 122 in subjects with active rheumatoid arthritis (RA) who are inadequately responding to methotrexate (MTX) treatment.

Timeline

Start
2014-07
Primary completion
2015-09
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject REMTOLUMAB Protein / enzyme biologic 60 mg Subcutaneous
Subject REMTOLUMAB Protein / enzyme biologic 120 mg Subcutaneous

Indications