drugset / Trial / NCT02675803

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of VAY736 in Rheumatoid Arthritis Patients

NCT02675803

Phase 1 Completed 65 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupTriple-blindTreatment

Summary

This study investigated the safety and tolerability of VAY736 administered as single ascending doses of intravenous infusion, subcutaneous injection and repeated subcutaneous injections in rheumatoid arthritis patients.

Timeline

Start
2010-12-20
Primary completion
2018-01-22
Completion
2018-01-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Ianalumab Monoclonal antibody Intravenous

Indications