Difference between revisions of "Alectinib (Alecensa)"

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*12/11/2015: Granted accelerated FDA approval for the treatment of patients with [[Biomarkers#ALK|anaplastic lymphoma kinase (ALK)]]-[[Biomarkers#Rearrangement|positive]] [[Contexts#Metastatic|metastatic]] [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] who have progressed on or are intolerant to [[Crizotinib (Xalkori)|crizotinib]]. ''(Based on [https://clinicaltrials.gov/ct2/show/NCT01588028 NP28761] and [https://clinicaltrials.gov/ct2/show/NCT01801111 NP28673])''
 
*12/11/2015: Granted accelerated FDA approval for the treatment of patients with [[Biomarkers#ALK|anaplastic lymphoma kinase (ALK)]]-[[Biomarkers#Rearrangement|positive]] [[Contexts#Metastatic|metastatic]] [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]] who have progressed on or are intolerant to [[Crizotinib (Xalkori)|crizotinib]]. ''(Based on [https://clinicaltrials.gov/ct2/show/NCT01588028 NP28761] and [https://clinicaltrials.gov/ct2/show/NCT01801111 NP28673])''
 
*11/6/2017: Granted regular FDA approval for treatment of patients with [[Biomarkers#ALK|anaplastic lymphoma kinase (ALK)]]-[[Biomarkers#Rearrangement|positive]] [[Contexts#Metastatic|metastatic]] [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]], as detected by an FDA-approved test. ''(Converted to regular approval; prior crizotinib exposure requirement removed; based on [https://clinicaltrials.gov/ct2/show/NCT02075840 ALEX])''
 
*11/6/2017: Granted regular FDA approval for treatment of patients with [[Biomarkers#ALK|anaplastic lymphoma kinase (ALK)]]-[[Biomarkers#Rearrangement|positive]] [[Contexts#Metastatic|metastatic]] [[Non-small_cell_lung_cancer|non-small cell lung cancer (NSCLC)]], as detected by an FDA-approved test. ''(Converted to regular approval; prior crizotinib exposure requirement removed; based on [https://clinicaltrials.gov/ct2/show/NCT02075840 ALEX])''
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==History of changes in EMA indication==
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*2/16/2017: Initial marketing authorization as Alecensa.
  
 
==Also known as==
 
==Also known as==
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[[Category:Non-small cell lung cancer medications]]
 
[[Category:Non-small cell lung cancer medications]]
  
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[[Category:EMA approved in 2017]]
 
[[Category:FDA approved in 2015]]
 
[[Category:FDA approved in 2015]]

Revision as of 02:37, 5 December 2021

General information

Class/mechanism: Tyrosine kinase inhibitor; inhibits anaplastic lymphoma kinase (ALK). Alectinib and its metabolite M4 inhibit ALK phosphorylation and ALK-mediated activation of the downstream signaling proteins STAT3 and AKT, which results in decreased growth of tumor cells which have ALK fusions, amplifications, or activating mutations.[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

History of changes in EMA indication

  • 2/16/2017: Initial marketing authorization as Alecensa.

Also known as

  • Code names: AF802, AF-802, CH5424802, RG7853, RO5424802, UNII-LIJ4CT1Z3Y
  • Brand names: Alecensa, Alecinix, Alecnib

References