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Relugolix/Estradiol/Norethisterone Acetate: A Review in Endometriosis-Associated Pain.

Authors :
Blair HA
Source :
Drugs [Drugs] 2024 Apr; Vol. 84 (4), pp. 449-457. Date of Electronic Publication: 2024 Apr 09.
Publication Year :
2024

Abstract

An oral fixed-dose combination of relugolix/estradiol/norethisterone (also known as norethindrone) acetate [Myfembree <superscript>®</superscript> (USA); Ryeqo <superscript>®</superscript> (EU)] (hereafter referred to as relugolix combination therapy) has been approved in the USA for the management of moderate to severe pain associated with endometriosis in premenopausal women and in the EU for the symptomatic treatment of endometriosis in adult women of reproductive age with a history of previous medical or surgical treatment for their endometriosis. The gonadotropin-releasing hormone (GnRH) receptor antagonist relugolix decreases estradiol and progesterone levels, while the addition of estradiol/norethisterone acetate mitigates hypoestrogenic effects including bone mineral density (BMD) loss and vasomotor symptoms. In two pivotal phase III trials, relugolix combination therapy significantly improved dysmenorrhoea and non-menstrual pelvic pain in premenopausal women with moderate to severe endometriosis. The combination also reduced overall pelvic pain and dyspareunia, reduced analgesic and opioid use, and improved health-related quality of life. The efficacy of relugolix combination therapy was sustained over the longer term (up to 2 years). Relugolix combination therapy was generally well tolerated and BMD loss over time was minimal. With the convenience of a once daily oral dosing regimen, relugolix combination therapy is a valuable addition to the options currently available for the management of endometriosis-associated pain.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)

Details

Language :
English
ISSN :
1179-1950
Volume :
84
Issue :
4
Database :
MEDLINE
Journal :
Drugs
Publication Type :
Academic Journal
Accession number :
38592603
Full Text :
https://doi.org/10.1007/s40265-024-02018-3