Drug class
LHrH(GNrH) Agonist Analog Pituitary Suppressants
Luteinizing hormone-releasing hormone (gonadotropin-releasing hormone) agonist analog pituitary suppressants are synthetic peptide derivatives that modulate the hypothalamic-pituitary-gonadal axis. Read more about LHrH(GNrH) Agonist Analog Pituitary Suppressants
38 drugs in this class 18 manufacturers
Drugs in LHrH(GNrH) Agonist Analog Pituitary Suppressants
SUPPRELIN LA (histrelin acetate)
LEUPROLIDE ACETATE
LEUPROLIDE ACETATE
SYNAREL (nafarelin acetate)
ZOLADEX (goserelin acetate)
ORILISSA (elagolix sodium)
ORIAHNN (elagolix sodium/estradiol/norethindrone acetate)
TRELSTAR (triptorelin pamoate)
Luteinizing hormone-releasing hormone (gonadotropin-releasing hormone) agonist analog pituitary suppressants are synthetic peptide derivatives that modulate the hypothalamic-pituitary-gonadal axis.
Although an initial administration induces a transient surge in gonadotropin release, chronic and continuous exposure paradoxically downregulates and desensitizes pituitary receptors, profoundly suppressing luteinizing hormone and follicle-stimulating hormone secretion.
This reversible inhibition depresses circulating sex hormones to castrate or postmenopausal levels, halting hormone-driven cellular proliferation.
Consequently, these agents serve as pivotal therapies in hormone-dependent oncology settings such as advanced prostate cancer and premenopausal breast cancer, as well as in benign sex-steroid-dependent disorders including endometriosis, uterine leiomyomas, and central precocious puberty.
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fda.gov
Luteinizing hormone-releasing hormone (gonadotropin-releasing hormone) agonist analog pituitary suppressants are synthetic peptide derivatives that modulate the hypothalamic-pituitary-gonadal axis
-
nih.gov
Luteinizing hormone-releasing hormone (gonadotropin-releasing hormone) agonist analog pituitary suppressants are synthetic peptide derivatives that modulate the hypothalamic-pituitary-gonadal axis Consequently, these agents serve as pivotal therapies in hormone-dependent oncology settings such as advanced prostate cancer and premenopausal breast cancer, as well as in benign sex-steroid-dependent disorders including endometriosis, uterine leiomyomas, and central precocious puberty
-
fda.gov
Although an initial administration induces a transient surge in gonadotropin release, chronic and continuous exposure paradoxically downregulates and desensitizes pituitary receptors, profoundly suppressing luteinizing hormone and follicle-stimulating hormone secretion This reversible inhibition depresses circulating sex hormones to castrate or postmenopausal levels, halting hormone-driven cellular proliferation
-
nih.gov
Although an initial administration induces a transient surge in gonadotropin release, chronic and continuous exposure paradoxically downregulates and desensitizes pituitary receptors, profoundly suppressing luteinizing hormone and follicle-stimulating hormone secretion
-
nih.gov
This reversible inhibition depresses circulating sex hormones to castrate or postmenopausal levels, halting hormone-driven cellular proliferation
-
lbbc.org
Consequently, these agents serve as pivotal therapies in hormone-dependent oncology settings such as advanced prostate cancer and premenopausal breast cancer, as well as in benign sex-steroid-dependent disorders including endometriosis, uterine leiomyomas, and central precocious puberty
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