Difference between revisions of "Ponatinib (Iclusig)"

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m (Text replacement - "[[Category:Drugs FDA" to "[[Category:FDA")
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*10/31/2013: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm373072.htm Suspended by FDA] because of the risk of life-threatening blood clots and severe narrowing of blood vessels.
 
*10/31/2013: [http://www.fda.gov/Drugs/InformationOnDrugs/ApprovedDrugs/ucm373072.htm Suspended by FDA] because of the risk of life-threatening blood clots and severe narrowing of blood vessels.
 
*12/20/2013: [http://www.iclusigrems.com/ REMS] program put in place and medication is once again available.
 
*12/20/2013: [http://www.iclusigrems.com/ REMS] program put in place and medication is once again available.
*11/29/2016: FDA granted full approval "for the treatment of adult patients with chronic-phase, accelerated-phase, or blast-phase [[Chronic myelogenous leukemia | chronic myeloid leukemia (CML)]] or Philadelphia chromosome–positive [[B-cell_acute_lymphoblastic_leukemia,_Ph-positive | acute lymphoblastic leukemia (ALL)]] for whom no other tyrosine kinase inhibitor therapy is indicated; and for the treatment of adult patients with T315I­–positive CML (chronic phase, accelerated phase, or blast phase) or T315I­-positive, Philadelphia chromosome–positive ALL."
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*11/29/2016: FDA granted full approval "for the treatment of adult patients with chronic-phase, accelerated-phase, or blast-phase [[Chronic myelogenous leukemia | chronic myeloid leukemia (CML)]] or [[Biomarkers#BCR-ABL1|Philadelphia chromosome]]–positive [[B-cell_acute_lymphoblastic_leukemia,_Ph-positive | acute lymphoblastic leukemia (ALL)]] for whom no other tyrosine kinase inhibitor therapy is indicated; and for the treatment of adult patients with [[Biomarkers#BCR-ABL1|T315I]]­–positive [[chronic myelogenous leukemia|CML]] (chronic phase, accelerated phase, or blast phase) or [[Biomarkers#BCR-ABL1|T315I]]­-positive, [[Biomarkers#BCR-ABL1|Philadelphia chromosome]]–positive [[B-cell_acute_lymphoblastic_leukemia,_Ph-positive|ALL]]."
  
 
==Also known as==
 
==Also known as==

Revision as of 23:32, 8 January 2020

General information

Class/mechanism: Tyrosine kinase inhibitor with multiple targets, including Bcr-Abl tyrosine kinase, the constitutively active tyrosine kinase resulting from the Philadelphia chromosome abnormality in CML, as well as VEGFR, PDGFR, FGFR, the SRC kinases, KIT, EPH receptors, RET, TIE2, and FLT3. Ponatinib is active against the Bcr-Abl T315I mutation.[1][2][3][4]
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 used

Patient drug information

History of changes in FDA indication

Also known as

  • Code name: AP24534
  • Generic name: ponatinib hydrochloride
  • Brand name: Iclusig

References