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Shandong Boan says China regulator approves expanded Boluojia use for bone metastases, multiple myeloma
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Shandong Boan says China regulator approves expanded Boluojia use for bone metastases, multiple myeloma
  • China’s NMPA cleared a supplemental filing for Boluojia (denosumab) 120 mg to treat bone metastases from solid tumors or multiple myeloma.
  • The label expansion targets prevention of skeletal-related events, a larger oncology use than its May 2024 China approval in giant cell tumor of bone.
  • Boluojia is a biosimilar of Amgen’s Xgeva; Xgeva logged about USD 2.08 billion in 2025 sales, including about USD 306 million in China.


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Shandong Boan Biotechnology Co. Ltd. published the original content used to generate this news brief via IIS, the regulatory disclosure system operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20260526-12170395), on May 26, 2026, and is solely responsible for the information contained therein.

Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
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