drugset / Trial / NCT02962895
Safety and Efficacy of VAY736 in Patients With Primary Sjogren's Syndrome (pSS)
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study was to determine the dose-response relationship of VAY736 for key efficacy and safety parameters
Timeline
- Start
- 2017-06-27
- Primary completion
- 2020-06-30
- Completion
- 2021-09-23
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ianalumab | Monoclonal antibody | 5 mg | Subcutaneous |
| Subject | Ianalumab | Monoclonal antibody | 50 mg | Subcutaneous |
| Subject | Ianalumab | Monoclonal antibody | 150 mg | Subcutaneous |
| Subject | Ianalumab | Monoclonal antibody | 300 mg | Subcutaneous |