Difference between revisions of "Dacomitinib (Vizimpro)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
 
*9/27/2018: Initial approval for the first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] with [[Biomarkers#EGFR|epidermal growth factor receptor (EGFR)]] [[Biomarkers#Exon_19|exon 19]] [[#Biomarkers_Structural Variant|deletion]] or [[Biomarkers#L858R|exon 21 L858R substitution]] mutations.
 
*9/27/2018: Initial approval for the first-line treatment of patients with metastatic [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] with [[Biomarkers#EGFR|epidermal growth factor receptor (EGFR)]] [[Biomarkers#Exon_19|exon 19]] [[#Biomarkers_Structural Variant|deletion]] or [[Biomarkers#L858R|exon 21 L858R substitution]] mutations.
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== Patient Drug Information==
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*[https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/211288s000lbl.pdf Dacomitinib (Vizimpro) Package Insert]<ref>[https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/211288s000lbl.pdf Dacomitinib (Vizimpro) Package Insert]</ref>
  
 
==Also known as==
 
==Also known as==

Revision as of 10:39, 4 April 2021

Mechanism of action

From the NCI Drug Dictionary: An orally bioavailable, highly selective, second-generation small-molecule inhibitor of the pan-epidermal growth factor receptor (EGFR) family of tyrosine kinases (ErbB family) with potential antineoplastic activity. Dacomitinib specifically and irreversibly binds to and inhibits human EGFR subtypes, resulting in inhibition of proliferation and induction of apoptosis in EGFR-expressing tumor cells.

Diseases for which it is approved

History of changes in FDA indication

Patient Drug Information

Also known as

  • Code name: PF-00299804
  • Brand name: Vizimpro