drugset / Trial / NCT05039190

Evaluate the Efficacy and Safety of HBM9161(HL161)Subcutaneous Injection in Patients With Generalized MG Patients

NCT05039190 ↗

Phase 3 Completed 132 enrolled Harbour BioMed (Guangzhou) Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary study objective: To confirm the efficacy of HBM9161 subcutaneous injection for the treatment of gMG in Chinese patients

Timeline

Start
2021-09-25
Primary completion
2023-01-14
Completion
2023-01-14

Drugs

EvaluationDrugModalityDoseRoute
Comparator Batoclimab Monoclonal antibody 680 mg Subcutaneous

Indications