[ET Net News Agency, 21 January 2022] BeiGene, Ltd. (06160) said the Center for Drug
Evaluation (CDE) of the China National Medical Products Administration (NMPA) has accepted
a supplemental new drug application (sNDA) for BeiGene's BTK inhibitor BRUKINSA
(zanubrutinib) as a treatment for adult patients with Waldenstrom's macroglobulinemia
(WM).
BRUKINSA is a small molecule inhibitor of Bruton's tyrosine kinase (BTK) discovered by
BeiGene scientists that is currently being evaluated globally in a broad clinical program
as a monotherapy and in combination with other therapies to treat various B-cell
malignancies. (RC)