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The European Commission has given approval for BeiGene’s TEVIMBRA to be used as the initial treatment for advanced or metastatic esophageal squamous cell carcinoma and gastric or gastroesophageal junction cancer.

BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160; SSE: 688235), a global oncology company that intends to change its name to BeOne Medicines, today announced that the European Commission has approved…

Read More: https://www.businesswire.com/news/home/20241127759978/en/

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