GONADOTROPIN-RELEASING-HORMONE AGONISTS - A GUIDE TO USE AND SELECTION

Authors
Citation
M. Filicori, GONADOTROPIN-RELEASING-HORMONE AGONISTS - A GUIDE TO USE AND SELECTION, Drugs, 48(1), 1994, pp. 41-58
Citations number
175
Categorie Soggetti
Pharmacology & Pharmacy",Toxicology
Journal title
DrugsACNP
ISSN journal
00126667
Volume
48
Issue
1
Year of publication
1994
Pages
41 - 58
Database
ISI
SICI code
0012-6667(1994)48:1<41:GA-AGT>2.0.ZU;2-1
Abstract
The development of superactive analogues of gonadatrophin-releasing ho rmone (GnRH) represents one of the most important new pharmaceutical c ontributions of the last 2 decades. This class of drugs is now availab le worldwide and is successfully employed in the management of precoci ous puberty, ovulation induction, prostatic cancer, premenopausal brea st cancer, endometriosis, uterine leiomyoma, and for the preparation o f female patients undergoing laparotomic, vaginal or endoscopic surger y. GnRH agonists art also applied with some success in other clinical conditions such as catamenial disorders, hyperandrogenism and menometr orrhagia. Studies are under way to identify other potential clinical a pplications such as other forms of cancer.