drugset / Trial / NCT04227470

A Study of HBM9161 in NMOSD Patients

NCT04227470 ↗

Phase 1 Completed 9 enrolled Harbour BioMed (Guangzhou) Co. Ltd.
NaSequentialOpen-labelTreatment

Summary

Primary Objectives:To investigate the safety and tolerability of HBM 9161 in patients with attack of NMOSD in China

Timeline

Start
2020-03-31
Primary completion
2021-12-03
Completion
2021-12-24

Drugs

EvaluationDrugModalityDoseRoute
Subject Batoclimab Monoclonal antibody 340 mg Subcutaneous
Subject Batoclimab Monoclonal antibody 680 mg Subcutaneous

Indications