Difference between revisions of "Enasidenib (Idhifa)"

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==Mechanism of action==
 
==Mechanism of action==
IDH2 inhibitor
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From the [https://www.cancer.gov/publications/dictionaries/cancer-drug?cdrid=752247 NCI Drug Dictionary]]: An orally available inhibitor of isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity. Upon administration, enasidenib specifically inhibits IDH2 in the mitochondria, which inhibits the formation of 2-hydroxyglutarate (2HG).
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==Diseases for which it is used==
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*[[Acute myeloid leukemia]]
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==History of changes in FDA indication==
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*8/1/2017: Granted [https://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm569482.htm FDA regular approval] "for the treatment of adult patients with relapsed or refractory [[acute myeloid leukemia|acute myeloid leukemia with an isocitrate dehydrogenase-2 (IDH2) mutation]] as detected by an FDA-approved test.
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==Also known as==
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AG-221, CC-90007
  
 
[[Category:Drug index]]
 
[[Category:Drug index]]
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[[Category:Oral medications]]
 
[[Category:Chemotherapy]]
 
[[Category:Chemotherapy]]
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[[Category:Mutation-specific drugs]]
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[[Category:Acute myeloid leukemia medications]]
  
 
[[Category:Enzyme inhibitors]]
 
[[Category:Enzyme inhibitors]]
 
[[Category:IDH2 inhibitors]]
 
[[Category:IDH2 inhibitors]]
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[[Category:Drugs FDA approved in 2017]]

Revision as of 13:35, 2 August 2017

Mechanism of action

From the NCI Drug Dictionary]: An orally available inhibitor of isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity. Upon administration, enasidenib specifically inhibits IDH2 in the mitochondria, which inhibits the formation of 2-hydroxyglutarate (2HG).

Diseases for which it is used

History of changes in FDA indication

Also known as

AG-221, CC-90007