The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles

Abstract Purpose Relugolix is an oral gonadotropin‐releasing hormone antagonist (GnRHant), which was first introduced in 2019. This study investigated the effects of the conventional injectable GnRHant formulation and this new oral GnRHant formulation on controlled ovarian stimulation (COS) cycles....

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Main Authors: Shinnosuke Komiya, Tomoko Tsuzuki‐Nakao, Yoshiko Asai, Tomoko Inoue, Yoshiharu Morimoto, Hidetaka Okada
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Reproductive Medicine and Biology
Subjects:
Online Access:https://doi.org/10.1002/rmb2.12448
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author Shinnosuke Komiya
Tomoko Tsuzuki‐Nakao
Yoshiko Asai
Tomoko Inoue
Yoshiharu Morimoto
Hidetaka Okada
author_facet Shinnosuke Komiya
Tomoko Tsuzuki‐Nakao
Yoshiko Asai
Tomoko Inoue
Yoshiharu Morimoto
Hidetaka Okada
author_sort Shinnosuke Komiya
collection DOAJ
description Abstract Purpose Relugolix is an oral gonadotropin‐releasing hormone antagonist (GnRHant), which was first introduced in 2019. This study investigated the effects of the conventional injectable GnRHant formulation and this new oral GnRHant formulation on controlled ovarian stimulation (COS) cycles. Methods Relugolix was administered in 126 cycles and conventional GnRHant injection was administered in 658 cycles (controls). The follicle stimulation was performed by an antagonist method, and for final oocyte maturation, recombinant human chorionic gonadotropin (rHCG), or gonadotropin‐releasing hormone agonist (GnRHa), or both (dual trigger) were selected. The number of retrieved oocytes was counted and then they were evaluated for subsequent development up to cleavage stage. Results The number of retrieved oocytes which was the primary outcome of this research was affected by the combination of GnRHant type and the final oocyte maturation agent. The combination of relugolix and a GnRHa trigger showed a significantly lower number of retrieved oocytes (p < 0.001) than the other combinations. Conclusions Relugolix is a new option for COS cycles, but should be carefully combined with the final maturation agent. Clinical trial approval This study was conducted after approval by the Medical Corporation Sankeikai Institutional Ethics Committee (approval number: 2019‐34).
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spelling doaj.art-5a86fefd6c8c476d9c9a863cf4984d7b2022-12-27T13:54:58ZengWileyReproductive Medicine and Biology1445-57811447-05782022-01-01211n/an/a10.1002/rmb2.12448The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cyclesShinnosuke Komiya0Tomoko Tsuzuki‐Nakao1Yoshiko Asai2Tomoko Inoue3Yoshiharu Morimoto4Hidetaka Okada5Department of Obstetrics and Gynecology Kansai Medical University Graduate School of Medicine Osaka JapanDepartment of Obstetrics and Gynecology Kansai Medical University Graduate School of Medicine Osaka JapanHORAC Grand Front Osaka Clinic Osaka JapanHORAC Grand Front Osaka Clinic Osaka JapanHORAC Grand Front Osaka Clinic Osaka JapanDepartment of Obstetrics and Gynecology Kansai Medical University Graduate School of Medicine Osaka JapanAbstract Purpose Relugolix is an oral gonadotropin‐releasing hormone antagonist (GnRHant), which was first introduced in 2019. This study investigated the effects of the conventional injectable GnRHant formulation and this new oral GnRHant formulation on controlled ovarian stimulation (COS) cycles. Methods Relugolix was administered in 126 cycles and conventional GnRHant injection was administered in 658 cycles (controls). The follicle stimulation was performed by an antagonist method, and for final oocyte maturation, recombinant human chorionic gonadotropin (rHCG), or gonadotropin‐releasing hormone agonist (GnRHa), or both (dual trigger) were selected. The number of retrieved oocytes was counted and then they were evaluated for subsequent development up to cleavage stage. Results The number of retrieved oocytes which was the primary outcome of this research was affected by the combination of GnRHant type and the final oocyte maturation agent. The combination of relugolix and a GnRHa trigger showed a significantly lower number of retrieved oocytes (p < 0.001) than the other combinations. Conclusions Relugolix is a new option for COS cycles, but should be carefully combined with the final maturation agent. Clinical trial approval This study was conducted after approval by the Medical Corporation Sankeikai Institutional Ethics Committee (approval number: 2019‐34).https://doi.org/10.1002/rmb2.12448fertilization in vitroinfertilityoocyte retrievalreproductive techniques, assistedsperm injections, intra‐cytoplasmic
spellingShingle Shinnosuke Komiya
Tomoko Tsuzuki‐Nakao
Yoshiko Asai
Tomoko Inoue
Yoshiharu Morimoto
Hidetaka Okada
The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
Reproductive Medicine and Biology
fertilization in vitro
infertility
oocyte retrieval
reproductive techniques, assisted
sperm injections, intra‐cytoplasmic
title The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
title_full The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
title_fullStr The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
title_full_unstemmed The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
title_short The novel oral gonadotropin‐releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
title_sort novel oral gonadotropin releasing hormone receptor antagonist relugolix is a new option for controlled ovarian stimulation cycles
topic fertilization in vitro
infertility
oocyte retrieval
reproductive techniques, assisted
sperm injections, intra‐cytoplasmic
url https://doi.org/10.1002/rmb2.12448
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