drugset / Trial / NCT04346888
A Study to Evaluate the Efficacy, Safety and PD and PK of HBM9161 in MG Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Batoclimab | Monoclonal antibody | 340 mg | Subcutaneous |
| Subject | Batoclimab | Monoclonal antibody | 680 mg | Subcutaneous |