Elagolix, a novel, orally bioavailable GnRH antagonist under investigation for the treatment of endometriosis-related pain

被引:18
作者
Ezzati, Mohammad [1 ]
Carr, Bruce R. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Obstet & Gynecol, Div Reprod Endocrinol & Infertil, 5323 Harry Hines Blvd, Dallas, TX 75390 USA
关键词
bone mineral density; elagolix; endometriosis; GnRH antagonists; medical treatment;
D O I
10.2217/WHE.14.68
中图分类号
R71 [妇产科学];
学科分类号
100211 [妇产科学];
摘要
Suppression of estrogen production and reduction of menstrual blood flow are the mainstays of medical treatment of endometriosis-related pain and have been traditionally achieved by methods such as combined hormonal contraception, progestins and GnRH analogs, all with comparable efficacies, though different side-effect profiles. Elagolix is the frontrunner among an emerging class of GnRH antagonists, which unlike their peptide predecessors has a nonpeptide structure resulting in its oral bioavailability. Phase I and II clinical trials have demonstrated safety of elagolix and its efficacy in partial and reversible suppression of ovarian estrogen production resulting in improvements in endometriosis-related pain. Phase III clinical trials are currently underway and elagolix may become a valuable addition to the armamentarium of pharmacological agents to treat endometriosis-related pain.
引用
收藏
页码:19 / 28
页数:10
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