Difference between revisions of "Radotinib (Supect)"

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'''Not currently approved in the United States.'''
 
==Mechanism of action==
 
==Mechanism of action==
Selective BCR-ABL1 tyrosine kinase inhibitor
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=723999 NCI Drug Dictionary]:  a second-generation tyrosine kinase inhibitor of Bcr-Abl fusion protein and the platelet-derived growth factor receptor (PDGFR), with potential antineoplastic activity. Upon administration, radotinib specifically inhibits the Bcr-Abl fusion protein, an abnormal enzyme expressed in Philadelphia chromosome-positive chronic myeloid leukemia (CML) cells. In addition, this agent also inhibits PDGFR thereby blocking PDGFR-mediated signal transduction pathways.
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==Diseases for which it is used==
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*[[Chronic myeloid leukemia]]
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==Also known as==
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*'''Code name:''' IY5511HCl
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*'''Brand name:''' Supect
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[[Category:Drugs]]
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[[Category:Oral medications]]
  
[[Category:Investigational]]
 
  
[[Category:Kinase inhibitors]]
 
 
[[Category:Bcr-Abl inhibitors]]
 
[[Category:Bcr-Abl inhibitors]]
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[[Category:PDGFR inhibitors]]
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[[Category:Chronic myeloid leukemia medications]]
  
[[Category:Chronic myelogenous leukemia medications]]
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[[Category:KFDA approved drugs]]

Latest revision as of 23:44, 26 September 2022

Not currently approved in the United States.

Mechanism of action

From the NCI Drug Dictionary: a second-generation tyrosine kinase inhibitor of Bcr-Abl fusion protein and the platelet-derived growth factor receptor (PDGFR), with potential antineoplastic activity. Upon administration, radotinib specifically inhibits the Bcr-Abl fusion protein, an abnormal enzyme expressed in Philadelphia chromosome-positive chronic myeloid leukemia (CML) cells. In addition, this agent also inhibits PDGFR thereby blocking PDGFR-mediated signal transduction pathways.

Diseases for which it is used

Also known as

  • Code name: IY5511HCl
  • Brand name: Supect