drugset / Trial / NCT04346888

A Study to Evaluate the Efficacy, Safety and PD and PK of HBM9161 in MG Patients

NCT04346888 ↗

Phase 2 Completed 30 enrolled Harbour BioMed (Guangzhou) Co. Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objectives: To investigate the efficacy of HBM9161 in patients with attack of MG in China

Timeline

Start
2020-07-23
Primary completion
2021-08-24
Completion
2021-08-24

Outcome

Met primary endpoint

release “Analysis of primary endpoint revealed both 340 and 680 mg of batoclimab treatment resulted in rapid, clinically meaningful, and statistically significant improvements over placebo” harbourbiomed.com ↗

Drugs

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