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ENDPOINTS 08/22/2019 10:35
→ BeiGene is getting a boost in its drive to field a rival to Imbruvica. The FDA has offered an to zanubrutinib , a BTK inhibitor that has posted positive results for mantle cell lymphoma. The PDUFA date lands on February 27, 2020. The drug scored breakthrough status at the beginning of the year. → BeiGene isn’t the only biopharma company to gain special regulatory status today. Mustang Bio and St. Jude Children’s Research Hospital announced that MB-107 , a lentiviral gene therapy for the treatment of , also known as bubble boy disease, has been granted Regenerative Medicine Advanced Therapy status. → Roche has been shaking up the hemophilia drug market with its blockbuster Hemlibra . And now the NHS in the UK is giving the pharma giant ano.

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