.Pharmacolibrary.Drugs.L_AntineoplasticAndImmunomodulatingAgents.L02A_HormonesAndRelatedAgents.L02AE04_Triptorelin.Triptorelin

Information

name:Triptorelin
ATC code:L02AE04
route:intramuscular
n-compartments1

Triptorelin is a synthetic decapeptide agonist analogue of gonadotropin-releasing hormone (GnRH), used primarily for the treatment of advanced prostate cancer, central precocious puberty, endometriosis, and uterine fibroids. It works by suppressing pituitary gonadotropin secretion, thus lowering sex hormone levels. Triptorelin is approved and in use today as a depot injection in various indications.

Pharmacokinetics

Pharmacokinetic parameters in adult males with advanced prostate cancer following single intramuscular dose of 3.75 mg depot formulation; non-compartmental analysis.

References

  1. Romero, E, et al., & Trocóniz, IF (2012). Pharmacokinetic/pharmacodynamic model of the testosterone effects of triptorelin administered in sustained release formulations in patients with prostate cancer. The Journal of pharmacology and experimental therapeutics 342(3) 788–798. DOI:10.1124/jpet.112.195560 PUBMED:https://pubmed.ncbi.nlm.nih.gov/22691297

  2. Tornøe, CW, et al., & Jonsson, EN (2007). Population pharmacokinetic/pharmacodynamic (PK/PD) modelling of the hypothalamic-pituitary-gonadal axis following treatment with GnRH analogues. British journal of clinical pharmacology 63(6) 648–664. DOI:10.1111/j.1365-2125.2006.02820.x PUBMED:https://pubmed.ncbi.nlm.nih.gov/17096678

  3. Lundström, EA, et al., & Porchet, HC (2009). Triptorelin 6-month formulation in the management of patients with locally advanced and metastatic prostate cancer: an open-label, non-comparative, multicentre, phase III study. Clinical drug investigation 29(12) 757–765. DOI:10.2165/11319690-000000000-00000 PUBMED:https://pubmed.ncbi.nlm.nih.gov/19888782

Revisions


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