drugset / Trial / NCT02962895

Safety and Efficacy of VAY736 in Patients With Primary Sjogren's Syndrome (pSS)

NCT02962895

Phase 2 Completed 190 enrolled Novartis Pharmaceuticals
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

EvaluationDrugModalityDoseRoute
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

Indications