Difference between revisions of "Sorafenib (Nexavar)"

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==History of changes in FDA indication==
 
==History of changes in FDA indication==
*12/20/2005: Approved for the treatment of patients with advanced [[Renal cell carcinoma | renal cell carcinoma (RCC)]]. ''(Based on TARGET<sub>RCC</sub>)''
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*2005-12-20: Approved for the treatment of patients with advanced [[Renal cell carcinoma | renal cell carcinoma (RCC)]]. ''(Based on TARGET<sub>RCC</sub>)''
*11/16/2007: Approved for the treatment of patients with unresectable [[Hepatocellular carcinoma| hepatocellular carcinoma (HCC)]]. ''(Based on SHARP)''
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*2007-11-16: Approved for the treatment of patients with unresectable [[Hepatocellular carcinoma| hepatocellular carcinoma (HCC)]]. ''(Based on SHARP)''
*11/22/2013: Approved for the treatment of locally recurrent or metastatic, progressive, [[Thyroid cancer, differentiated| differentiated thyroid carcinoma (DTC)]] refractory to radioactive iodine treatment. ''(Based on DECISION)''
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*2013-11-22: Approved for the treatment of locally recurrent or metastatic, progressive, [[Thyroid cancer, differentiated| differentiated thyroid carcinoma (DTC)]] refractory to radioactive iodine treatment. ''(Based on DECISION)''
  
 
==History of changes in EMA indication==
 
==History of changes in EMA indication==
*7/19/2006: Initial marketing authorization as Nexavar
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*2006-07-19: Initial marketing authorization as Nexavar
 
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==History of changes in Health Canada indication==
 +
*2006-07-28: Initial notice of compliance with conditions
 +
*2009-06-12: Conditions were met
 
==Also known as==
 
==Also known as==
 
*'''Code names:''' BAY 43-9006, BAY 54-9085
 
*'''Code names:''' BAY 43-9006, BAY 54-9085
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[[Category:EMA approved in 2006]]
 
[[Category:EMA approved in 2006]]
 
[[Category:FDA approved in 2005]]
 
[[Category:FDA approved in 2005]]
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[[Category:Health Canada approved in 2006]]

Revision as of 01:26, 31 March 2023

General information

Class/mechanism: Tyrosine kinase inhibitor that inhibits multiple kinases: RAF1, BRAF, KIT, FLT-3, RET, vascular endothelial growth factor receptors VEGFR-1, VEGFR-2, VEGFR-3, and platelet-derived growth factor receptor beta (PDGFR-B). Inhibition of these kinases disrupts angiogenesis, tumor cell signaling, and induces apoptosis.[1][2][3]
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.[1]

Diseases for which it is established (work in progress)

Diseases for which it is used

Patient drug information

History of changes in FDA indication

History of changes in EMA indication

  • 2006-07-19: Initial marketing authorization as Nexavar

History of changes in Health Canada indication

  • 2006-07-28: Initial notice of compliance with conditions
  • 2009-06-12: Conditions were met

Also known as

  • Code names: BAY 43-9006, BAY 54-9085
  • Brand names: Nexavar, Sorafenat, Soranib

References