Harbour BioMed Reports P-III Trial Results of Batoclimab for the Treatment of Generalized Myasthenia Gravis
Shots:
- The P-III clinical trial evaluates batoclimab (HBM9161), a fully human anti-FcRn mAb that blocks FcRn-IgG interactions in patients with gMG
- The trial met its 1EPs & 2EPs i.e., the therapy was found to be safe and well-tolerated & no new safety signal was observed while P-II study results showed that batoclimab can quickly and significantly alleviate patients’ symptoms and improve QoL
- In early 2021, Batoclimab received the Breakthrough Therapy Certificate from NMPA. Harbour BioMed & NBP Pharma collaborated to co-develop batoclimab in Great China & Harbour BioMed was responsible for developing & operating the full clinical trial of batoclimab for gMG in China
Ref: Harbour BioMed | Image: Harbour BioMed
Related Post:- Cullinan Oncology Entered into an Exclusive License with Harbour BioMed to Develop and Commercialize HBM7008 (CLN-418) in the US
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