Difference between revisions of "Zanubrutinib (Brukinsa)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
===[[Mantle cell lymphoma]]===
 
===[[Mantle cell lymphoma]]===
*11/14/2019: Accelerated approval for adult patients with [[mantle cell lymphoma|mantle cell lymphoma (MCL)]] who have received at least one prior therapy. ''(Based on BGB-3111-206)''
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*11/14/2019: Accelerated approval for adult patients with [[mantle cell lymphoma|mantle cell lymphoma (MCL)]] who have received at least one prior therapy. ''(Based on BGB-3111-AU-003 & BGB-3111-206)''
  
 
===[[Marginal zone lymphoma]]===
 
===[[Marginal zone lymphoma]]===

Revision as of 18:27, 11 July 2022

General information

Class/mechanism: BTK inhibitor
Route: PO
Extravasation: n/a

For conciseness and simplicity, HemOnc.org currently will focus on treatment regimens and not list information such as: renal/hepatic dose adjustments, metabolism (including CYP450), excretion, monitoring parameters (although this will be considered for checklists), or manufacturer. Instead, for the most current information, please refer to your preferred pharmacopeias such as Micromedex, Lexicomp, UpToDate (courtesy of Lexicomp), or the prescribing information.

Diseases for which it is established (work in progress)

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Mantle cell lymphoma

  • 11/14/2019: Accelerated approval for adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy. (Based on BGB-3111-AU-003 & BGB-3111-206)

Marginal zone lymphoma

Waldenström macroglobulinemia

Also known as

  • Code name: BGB-3111
  • Brand name: Brukinsa

References