Difference between revisions of "Zanubrutinib (Brukinsa)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
===[[Chronic lymphocytic leukemia]]===
 
===[[Chronic lymphocytic leukemia]]===
*1/19/2023: Approved for [[Chronic lymphocytic leukemia|chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL)]]. ''(Based on SEQUOIA<sub>CLL</sub>)''
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*2023-01-19: Approved for [[Chronic lymphocytic leukemia|chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL)]]. ''(Based on SEQUOIA<sub>CLL</sub>)''
 
===[[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-AU-003 & BGB-3111-206)''
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*2019-11-14: 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]]===
*9/14/2021: Accelerated approval for adult patients with relapsed or refractory [[Marginal zone lymphoma|marginal zone lymphoma (MZL)]] who have received at least one [[Regimen_classes#Anti-CD20-based_regimen|anti-CD20-based regimen]]. ''(Based on MAGNOLIA and BGB-3111-AU-003)''
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*2021-09-14: Accelerated approval for adult patients with relapsed or refractory [[Marginal zone lymphoma|marginal zone lymphoma (MZL)]] who have received at least one [[Regimen_classes#Anti-CD20-based_regimen|anti-CD20-based regimen]]. ''(Based on MAGNOLIA and BGB-3111-AU-003)''
  
 
===[[Waldenström macroglobulinemia]]===
 
===[[Waldenström macroglobulinemia]]===
*8/31/2021: Approved for adult patients with [[Waldenström macroglobulinemia|Waldenström’s macroglobulinemia (WM)]]. ''(Based on ASPEN)''
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*2021-08-31: Approved for adult patients with [[Waldenström macroglobulinemia|Waldenström’s macroglobulinemia (WM)]]. ''(Based on ASPEN)''
 
==History of changes in EMA indication==
 
==History of changes in EMA indication==
*11/22/2021: Initial authorization
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*2021-11-22: Initial authorization
  
 
==Also known as==
 
==Also known as==

Revision as of 18:50, 7 May 2023

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

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Chronic lymphocytic leukemia

Mantle cell lymphoma

  • 2019-11-14: 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

History of changes in EMA indication

  • 2021-11-22: Initial authorization

Also known as

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

References