drugset / Trial / NCT02713256

A Study to Evaluate the Safety and Effect of CFZ533 on Patients With Graves' Disease

NCT02713256

Phase 2 Completed 15 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

An open label study to evaluate the safety and efficacy of CFZ533 following 12 weeks treatment in patients with Graves' disease

Timeline

Start
2016-04-19
Primary completion
2017-04-24
Completion
2017-04-24

Drugs

EvaluationDrugModalityDoseRoute
Subject iscalimab Monoclonal antibody 10 mg/kg Intravenous

Indications