
FDA Approval for Zanubrutinib in Waldenstrom macroglobulinemia (WM)
According to BeiGene, the drug's manufacturer, the U.S. FDA has approved zanubrutinib (Brukinsa) capsules to treat adult patients with Waldenstrom macroglobulinemia (WM), a rare non-Hodgkin lymphoma. ...

USA: Approval of New Molecular Entity from 2001 to 2021
USA: Approval of New Molecular Entity from 2001 to 2021