drugset / Trial / NCT03052322
MSB11022 in Moderate to Severe Rheumatoid Arthritis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | EU-Humira | Unknown | 40 mg | Subcutaneous |
| Subject | MSB11022 | Unknown | 40 mg | Subcutaneous |