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Positive Ph III Results for Boan Biotech’s Denosumab Biosimilar

Feb 17, 2025

On 17 February 2025, Boan Biotech announced that the Journal of Bone Oncology published Phase III trial results for its biosimilar denosumab (Boluojia®/BA1102, formerly code-named LY01011), demonstrating comparable efficacy and safety to reference product, Amgen’s Xgeva®.  Boluojia® is reported to have met all primary and secondary endpoints.

Boluojia® was approved for marketing in China in May 2024 for the treatment of giant cell tumours of bone, following the approval of Mabwell’s Maiweijian™ in April 2024, which was the first Chinese approved denosumab biosimilar.