BeiGene Announces BRUKINSA™ (zanubrutinib) Is Approved in 50 Markets - News Summed Up

BeiGene Announces BRUKINSA™ (zanubrutinib) Is Approved in 50 Markets


BRUKINSA is supported by a broad clinical program which includes more than 3,900 subjects in 35 trials across 28 markets. Novartis and BeiGene also entered into a strategic commercial agreement through which BeiGene is promoting five approved Novartis Oncology products across designated regions of China. Drug InteractionsCYP3A Inhibitors: When BRUKINSA is co-administered with a strong CYP3A inhibitor, reduce BRUKINSA dose to 80 mg once daily. For coadministration with a moderate CYP3A inhibitor, reduce BRUKINSA dose to 80 mg twice daily. Specific PopulationsHepatic Impairment: The recommended dose of BRUKINSA for patients with severe hepatic impairment is 80 mg orally twice daily.


Source: The North Africa Journal June 13, 2022 11:52 UTC



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