Difference between revisions of "Idecabtagene vicleucel (Abecma)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
*3/26/2021: Approved for the treatment of adult patients with relapsed or refractory [[multiple myeloma]] after four or more prior lines of therapy, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody.
 
*3/26/2021: Approved for the treatment of adult patients with relapsed or refractory [[multiple myeloma]] after four or more prior lines of therapy, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody.
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== Patient Drug Information==
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*[https://www.fda.gov/media/147055/download idecabtagene vicleucel (Abecma) Package Insert]<ref>[https://www.fda.gov/media/147055/download idecabtagene vicleucel (Abecma) Package Insert]</ref>
  
 
==Also known as==
 
==Also known as==
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*'''Generic name:''' ide-cel
 
*'''Generic name:''' ide-cel
 
*'''Brand name:''' Abecma
 
*'''Brand name:''' Abecma
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==References==
  
 
[[Category:Chimeric antigen receptor T-cells]]
 
[[Category:Chimeric antigen receptor T-cells]]

Revision as of 11:17, 4 April 2021

Mechanism of action

Anti-BCMA CAR T-cells.

Diseases for which it is used

History of changes in FDA indication

  • 3/26/2021: Approved for the treatment of adult patients with relapsed or refractory multiple myeloma after four or more prior lines of therapy, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody.

Patient Drug Information

Also known as

  • Code name: bb2121
  • Generic name: ide-cel
  • Brand name: Abecma

References