drugset / Trial / NCT01873443

Long-Term Efficacy and Safety of CT-P10 in Patients With RA

NCT01873443

Phase 1 Completed 87 enrolled Celltrion
NaSingle-groupOpen-labelTreatment

Summary

This is an open-label, single-arm, multicenter, efficacy, and safety maintenance study of the Phase 1 Study CT-P10 1.1. This study is designed to assess the long-term efficacy and safety of CT-P10 co-administered with MTX and folic acid in patients with RA who have completed the scheduled visits in Study CT-P10 1.1

Timeline

Start
2013-05
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 1000 mg Intravenous
Background MTX Unknown 10 mg
Background MTX Unknown 25 mg
Background folic acid Other / unclassified 5 mg

Indications