Drug intelligence / Profile preview

degarelix

Development stage
Approved
Lead developer
Ferring Pharmaceuticals
Modality
Small Molecules, Peptides
Administration
Subcutaneous
01

Overview

Degarelix is a selective gonadotropin-releasing hormone (GnRH) receptor antagonist used primarily for androgen deprivation therapy in patients with prostate cancer. It competitively and reversibly binds to pituitary GnRH receptors, leading to rapid suppression of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which in turn reduces testosterone production by the testes. Unlike GnRH agonists, degarelix does not cause an initial surge in LH or testosterone levels ("flare"), making it advantageous for immediate testosterone suppression. It is administered as a subcutaneous injection and has demonstrated efficacy comparable to leuprolide but with a faster onset of action[1][4][8]. Degarelix was developed by Ferring Pharmaceuticals and is marketed under the brand name Firmagon[7].

Brand names
Firmagon费蒙格
Other names
醋酸地加瑞克Degarelix Acetate注射用醋酸地加瑞克
02

Targets

GnRHR (Gonadotropin-releasing hormone receptor)

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