drugset / Trial / NCT02565576

Safety,Tolerability,Pharmacokinetics and Efficacy of CFZ533 in Moderate to Severe Myasthenia Gravis

NCT02565576

Phase 2 Completed 44 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate safety, tolerability, pharmacokinetics/pharmacodynamics and efficacy of CFZ533 as an add-on therapy to standard of care in patients with moderate to severe myasthenia gravis (MG).

Timeline

Start
2015-09-29
Primary completion
2017-07-31
Completion
2017-12-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator iscalimab Monoclonal antibody