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European Commission Approves Tablet Formulation of BeOne Medicines’ BRUKINSA® for All Approved Indications

SAN CARLOS, Calif., August 21, 2025--BeOne Medicines Ltd. (Nasdaq: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the European Commission has approved a new film-coated tablet formulation of BRUKINSA® (zanubrutinib) for all approved indications.

articleBeone Medicines Ltd. Class AAugust 21, 20254/company/beigene-ltd/news/european-commission-approves-tablet-formulation-100000871
European Commission Approves Tablet Formulation of BeOne Medicines’ BRUKINSA® for All Approved Indications

About this update from Beone Medicines Ltd. Class A

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More updates from Beone Medicines Ltd. Class A

European Medicines Agencytablet formulationEuropean CommissionBRUKINSABeOne Medicines Ltd.BTKBeOneapproved indicationsBeOne Medicines