Difference between revisions of "Galeterone (TOK-001)"

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m (Text replacement - "please refer to your preferred pharmacopeias such as [http://www.thomsonhc.com/home/dispatch Micromedex], [https://online.lexi.com/lco/action/login UpToDate Lexidrug], [http://www.utdol.com/online/content/search.do UpToDate (courtesy of Lexicomp)], or the prescribing information" to "please refer to your preferred pharmacopeias or the prescribing information")
 
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==General information==
 
==General information==
Class/mechanism: Antiandrogen with multiple mechanisms of action: androgen receptor inhibitor (ARI), androgen biosynthesis inhibitor (CYP17 inhibitor), and accelerates degradation of the androgen receptor. Galeterone is believed to decrease prostate cancer proliferation and trigger cell death by interfering with testosterone-mediated pathways and signaling mechanisms used by prostate cancer cells.<ref>Robert B. Montgomery, Mario A. Eisenberger, Elisabeth I. Heath, A. Oliver Sartor, Franklin Chu, Neal D. Shore, William Jeffery Edenfield, Alan J. Koletsky, David Uri Lipsitz, James S. Cochran, Luke T. Nordquist, Jennifer Roberts, Mary-Ellen Taplin. Galeterone in men with CRPC: Results in four distinct patient populations from the ARMOR2 study. 2014 ASCO Annual Meeting abstract 5029. [http://meetinglibrary.asco.org/content/135176-144 link to abstract]</ref><ref>[http://www.ascopost.com/ViewNews.aspx?nid=20590 Galeterone Shows Activity in Variant Form of Castration-Resistant Prostate Cancer] The ASCO Post, 11/19/2014</ref>
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Class/mechanism: Antiandrogen with multiple mechanisms of action: androgen receptor inhibitor (ARI), androgen biosynthesis inhibitor (CYP17 inhibitor), and accelerates degradation of the androgen receptor. Galeterone is believed to decrease prostate cancer proliferation and trigger cell death by interfering with testosterone-mediated pathways and signaling mechanisms used by prostate cancer cells.<ref>Robert B. Montgomery, Mario A. Eisenberger, Elisabeth I. Heath, A. Oliver Sartor, Franklin Chu, Neal D. Shore, William Jeffery Edenfield, Alan J. Koletsky, David Uri Lipsitz, James S. Cochran, Luke T. Nordquist, Jennifer Roberts, Mary-Ellen Taplin. Galeterone in men with CRPC: Results in four distinct patient populations from the ARMOR2 study. 2014 ASCO Annual Meeting abstract 5029. [http://meetinglibrary.asco.org/content/135176-144 link to abstract]</ref><ref>[http://www.ascopost.com/ViewNews.aspx?nid=20590 Galeterone Shows Activity in Variant Form of Castration-Resistant Prostate Cancer] The ASCO Post, 11/19/2014</ref>
 
<br>Route: PO
 
<br>Route: PO
 
<br>Extravasation: n/a
 
<br>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 [http://www.thomsonhc.com/home/dispatch Micromedex], [http://online.lexi.com/ Lexicomp], [http://www.utdol.com/online/content/search.do UpToDate (courtesy of Lexicomp)], or the prescribing information.
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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 or the prescribing information.
  
 
==Patient drug information==
 
==Patient drug information==
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==Also known as==
 
==Also known as==
*'''Code names:''' AR-V7, VN/124-1
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*'''Code names:''' AR-V7, TOK-001, VN/124-1
  
 
==References==
 
==References==
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[[Category:Oral medications]]
 
[[Category:Oral medications]]
  
[[Category:Antiandrogens]]
 
 
[[Category:Steroidal androgen receptor inhibitors]]
 
[[Category:Steroidal androgen receptor inhibitors]]
[[Category:Steroid synthesis inhibitors]]
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[[Category:CYP17 inhibitors]]
  
 
[[Category:Halted drugs]]
 
[[Category:Halted drugs]]

Latest revision as of 01:06, 29 June 2024

General information

Class/mechanism: Antiandrogen with multiple mechanisms of action: androgen receptor inhibitor (ARI), androgen biosynthesis inhibitor (CYP17 inhibitor), and accelerates degradation of the androgen receptor. Galeterone is believed to decrease prostate cancer proliferation and trigger cell death by interfering with testosterone-mediated pathways and signaling mechanisms used by prostate cancer cells.[1][2]
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 or the prescribing information.

Patient drug information

No information available.

Also known as

  • Code names: AR-V7, TOK-001, VN/124-1

References

  1. Robert B. Montgomery, Mario A. Eisenberger, Elisabeth I. Heath, A. Oliver Sartor, Franklin Chu, Neal D. Shore, William Jeffery Edenfield, Alan J. Koletsky, David Uri Lipsitz, James S. Cochran, Luke T. Nordquist, Jennifer Roberts, Mary-Ellen Taplin. Galeterone in men with CRPC: Results in four distinct patient populations from the ARMOR2 study. 2014 ASCO Annual Meeting abstract 5029. link to abstract
  2. Galeterone Shows Activity in Variant Form of Castration-Resistant Prostate Cancer The ASCO Post, 11/19/2014