drugset / Trial / NCT03052322

MSB11022 in Moderate to Severe Rheumatoid Arthritis

NCT03052322

Phase 3 Completed 288 enrolled Fresenius Kabi SwissBioSim GmbH
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the efficacy, safety and immunogenicity of MSB11022 and Humira® in adult participants with rheumatoid arthritis (RA).

Timeline

Start
2017-01-31
Primary completion
2018-05-28
Completion
2018-08-27

Drugs

EvaluationDrugModalityDoseRoute
Comparator EU-Humira Unknown 40 mg Subcutaneous
Subject MSB11022 Unknown 40 mg Subcutaneous

Indications