Difference between revisions of "Histrelin (Vantas)"

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=Mechanism of action=
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==General information==
Histrelin acetate, an LH-RH agonist, acts as a potent inhibitor of gonadotropin secretion when given continuously in therapeutic doses. Both animal and human studies indicate that following an initial stimulatory phase, chronic, subcutaneous administration of histrelin acetate desensitizes responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.
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Class/mechanism: LH-RH agonist. Histrelin acetate inhibits gonadotropin secretion by desensitizing responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.<ref name="insert">[https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021732s015lbl.pdf Histrelin (Vantas) package insert]</ref><ref>[[:File:Histrelin.pdf | Histrelin (Vantas) package insert (locally hosted backup)]]</ref><ref>[http://www.vantasimplant.com/ Vantas implant manufacturer's website]</ref>
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<br>Route: SC
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<br>Extravasation: no information
  
=Diseases for which it is used=
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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.<ref name="insert"></ref>
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==Diseases for which it is used==
 
*[[Prostate cancer]]
 
*[[Prostate cancer]]
  
=History of changes in FDA indication=
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==History of changes in FDA indication==
*10/12/2004: Initial FDA approval "in the palliative treatment of advanced [[prostate cancer]]."
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*2004-10-12: Initial approval in the palliative treatment of advanced [[prostate cancer]]. ''(Based on Schlegel 2006)''
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==History of changes in Health Canada indication==
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*2006-03-10: Initial notice of compliance (unclear details)
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==Patient drug information==
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*[https://www.accessdata.fda.gov/drugsatfda_docs/label/2014/021732s015lbl.pdf Histrelin (Vantas) package insert]<ref name="insert"></ref>
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==Also known as==
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*'''Generic name:''' histrelin acetate
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*'''Brand names:''' Supprelin, Vantas
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==References==
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<references/>
  
[[Category:Drug index]]
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[[Category:Drugs]]
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[[Category:Subcutaneous medications]]
  
[[Category:Endocrine therapy]]
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[[Category:GnRH agonists]]
[[Category:LH-RH agonist]]
 
  
 
[[Category:Prostate cancer medications]]
 
[[Category:Prostate cancer medications]]
  
[[Category:Drugs FDA approved in 2004]]
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[[Category:FDA approved in 2004]]
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[[Category:Health Canada approved in 2006]]

Latest revision as of 01:03, 29 June 2024

General information

Class/mechanism: LH-RH agonist. Histrelin acetate inhibits gonadotropin secretion by desensitizing responsiveness of the pituitary gonadotropin which, in turn, causes a reduction in testicular steroidogenesis.[1][2][3]
Route: SC
Extravasation: no information

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.[1]

Diseases for which it is used

History of changes in FDA indication

  • 2004-10-12: Initial approval in the palliative treatment of advanced prostate cancer. (Based on Schlegel 2006)

History of changes in Health Canada indication

  • 2006-03-10: Initial notice of compliance (unclear details)

Patient drug information

Also known as

  • Generic name: histrelin acetate
  • Brand names: Supprelin, Vantas

References