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BeOne Medicines’ Brukinsa tablet formulation approved by European Commission

BeOne Medicines (ONC) announced that the European Commission has approved a new film-coated tablet formulation of Brukinsa – zanubrutinib – for all approved indications. The Brukinsa tablets are 160 mg each, allowing patients to halve their daily pill intake from four pills to two. Additionally, they are smaller than the capsules and have film coatings, which make them easier to swallow. Brukinsa is designed to deliver complete and sustained inhibition of the BTK protein and has been demonstrated to inhibit the proliferation of malignant B cells within a number of disease-relevant tissues.

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