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See the DrugPatentWatch profile for Brukinsa
Brukinsa (zanubrutinib) received FDA approval on November 14, 2019. [1]
The FDA initially approved Brukinsa for the treatment of adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. [1]
The provided information only specifies the initial FDA approval date; it does not include later approvals or indication expansions. [1]
You can cross-check the approval date in DrugPatentWatch’s listing for Brukinsa here: [1].
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