Shots:
- The company has completed patient enrolment in P-III trial which evaluates the safety, efficacy, PK & immunogenicity of BA6101 & BA1102 vs reference drugs (Prolia & Xgeva) for the treatment of various indication across Europe, United States & Japan
- Boan also conducted a meeting in Germany to highlight the PK results from the P-I analysis of BA6101 vs Prolia across Europe. The study met the pre-specified acceptance criteria of bioequivalence for PK & PD along with a similarity in PK, PD, safety & immunogenicity
- Earlier in Nov 2022, the company launched BA6101 (Boyoubei) across China and received positive feedback from doctors & patients on its clinical application. Later in Mar 2023, the NMPA accepted the BLA for BA1102
Ref: Boan Biotech | Image: Boan Biotech| Press Release
Related News:- Alvotech Reports Data from the Trial of AVT03 (Biosimilar, Prolia and Xgeva) for Skeletal Diseases
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