Difference between revisions of "Tafasitamab (Monjuvi)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
*7/31/2020: Granted accelerated approval in combination with lenalidomide for adult patients with relapsed or refractory [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL) not otherwise specified]], including [[Transformed lymphoma|DLBCL arising from low grade lymphoma]], and who are not eligible for autologous stem cell transplant. ''(Based on L-MIND)''
 
*7/31/2020: Granted accelerated approval in combination with lenalidomide for adult patients with relapsed or refractory [[Diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL) not otherwise specified]], including [[Transformed lymphoma|DLBCL arising from low grade lymphoma]], and who are not eligible for autologous stem cell transplant. ''(Based on L-MIND)''
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==History of changes in EMA indication==
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*8/26/2021: Initial conditional approval as Minjuvi
  
 
==Also known as==
 
==Also known as==
 
*'''Code names:''' MOR208, MOR00208, XmAb5574
 
*'''Code names:''' MOR208, MOR00208, XmAb5574
 
*'''Generic name:''' tafasitamab-cxix
 
*'''Generic name:''' tafasitamab-cxix
*'''Brand name:''' Monjuvi
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*'''Brand name:''' Minjuvi, Monjuvi
  
 
[[Category:Drugs]]
 
[[Category:Drugs]]
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[[Category:Transformed lymphoma medications]]
 
[[Category:Transformed lymphoma medications]]
  
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[[Category:EMA approved in 2021]]
 
[[Category:FDA approved in 2020]]
 
[[Category:FDA approved in 2020]]

Revision as of 02:31, 31 December 2022

Mechanism of action

Anti-CD19 antibody with an engineered Fc region to enhance Fcγ receptor binding affinity

Diseases for which it is used

History of changes in FDA indication

History of changes in EMA indication

  • 8/26/2021: Initial conditional approval as Minjuvi

Also known as

  • Code names: MOR208, MOR00208, XmAb5574
  • Generic name: tafasitamab-cxix
  • Brand name: Minjuvi, Monjuvi