Difference between revisions of "Polatuzumab vedotin (Polivy)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*6/10/2019: Initial approval in combination with bendamustine and a rituximab product for adult patients with relapsed or refractory [[diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL), not otherwise specified]], after at least two prior therapies.
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*6/10/2019: Initial approval in combination with bendamustine and a rituximab product for adult patients with relapsed or refractory [[diffuse large B-cell lymphoma|diffuse large B-cell lymphoma (DLBCL), not otherwise specified]], after at least two prior therapies. ''(Based on GO29365)''
  
 
==Also known as==
 
==Also known as==
*'''Code names:''' DCDS4501A
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*'''Code name:''' DCDS4501A
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*'''Generic name:''' polatuzumab vedotin-piiq
 
*'''Brand name:''' Polivy  
 
*'''Brand name:''' Polivy  
  
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[[Category:FDA approved in 2019]]
 
[[Category:FDA approved in 2019]]
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[[Category:Genentech product]]

Revision as of 22:08, 10 May 2021

General information

Class/mechanism from the NCI Drug Dictionary: An antibody-drug conjugate (ADC) composed of a monoclonal antibody directed against B-cell antigen receptor complex-associated protein beta chain (CD79B) conjugated, via a protease-cleavable peptide linker, to monomethyl auristatin E (MMAE), an auristatin derivative and a potent microtubule inhibitor, with potential antineoplastic activity. Upon administration, polatuzumab vedotin selectively binds to CD79B, a protein which is abundantly expressed on the surface of B-cells. Upon internalization and proteolytic cleavage, MMAE binds to tubulin and inhibits its polymerization, resulting in G2/M phase arrest and tumor cell apoptosis.
Route: IV
Extravasation: neutral

Diseases for which it is used

Patient drug information

History of changes in FDA indication

Also known as

  • Code name: DCDS4501A
  • Generic name: polatuzumab vedotin-piiq
  • Brand name: Polivy

References