Scientific article
Open access

Pharmacological profile of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix

Published inThe Journal of pharmacology and experimental therapeutics, vol. 301, no. 1, p. 95-102
Publication date2002

We describe the pharmacological profile in rats and monkeys of degarelix (FE200486), a member of a new class of long-acting gonadotropin-releasing hormone (GnRH) antagonists. At single subcutaneous injections of 0.3 to 10 microg/kg in rats, degarelix produced a dose-dependent suppression of the pituitary-gonadal axis as revealed by the decrease in plasma luteinizing hormone (LH) and testosterone levels. Duration of LH suppression increased with the dose: in the rat, significant suppression of LH lasted 1, 2, and 7 days after a single subcutaneous injection of degarelix at 12.5, 50, or 200 microg/kg, respectively. Degarelix fully suppressed plasma LH and testosterone levels in the castrated and intact rats as well as in the ovariectomized rhesus monkey for more than 40 days after a single 2-mg/kg subcutaneous injection. In comparative experiments, degarelix showed a longer duration of action than the recently developed GnRH antagonists abarelix, ganirelix, cetrorelix, and azaline B. The in vivo mechanism of action of degarelix was consistent with competitive antagonism, and the prolonged action of degarelix was paralleled by continued presence of radioimmunoassayable degarelix in the general circulation. In contrast to cetrorelix and similarly to ganirelix and abarelix, degarelix had only weak histamine-releasing properties in vitro. These results demonstrate that the unique and favorable pharmacological properties of degarelix make it an ideal candidate for the management of sex steroid-dependent pathologies requiring long-term inhibition of the gonadotropic axis.

  • Animals
  • Female
  • Gonadal Steroid Hormones/physiology
  • Gonadotropin-Releasing Hormone/antagonists & inhibitors
  • Gonads/drug effects/physiology
  • Histamine Release/drug effects
  • Hormone Antagonists/administration & dosage/pharmacokinetics/pharmacology
  • Injections, Intravenous
  • Injections, Subcutaneous
  • Luteinizing Hormone/blood
  • Macaca mulatta
  • Male
  • Mast Cells/drug effects/metabolism
  • Oligopeptides/administration & dosage/pharmacokinetics/pharmacology
  • Orchiectomy
  • Pituitary Gland/drug effects/physiology
  • Rats
  • Rats, Sprague-Dawley
  • Testosterone/blood
Citation (ISO format)
BROQUA, Pierre et al. Pharmacological profile of a new, potent, and long-acting gonadotropin-releasing hormone antagonist: degarelix. In: The Journal of pharmacology and experimental therapeutics, 2002, vol. 301, n° 1, p. 95–102.
Main files (1)
Article (Published version)
ISSN of the journal0022-3565

Technical informations

Creation04/23/2015 1:10:00 PM
First validation04/23/2015 1:10:00 PM
Update time03/14/2023 11:15:38 PM
Status update03/14/2023 11:15:37 PM
Last indexation01/16/2024 5:56:13 PM
All rights reserved by Archive ouverte UNIGE and the University of GenevaunigeBlack