Drug intelligence / Profile preview

menotropin + GnRH antagonist

Development stage
Unknown
Lead developer
Ferring Pharmaceuticals
Modality
Recombinant Proteins and Enzymes, Peptides
Administration
Subcutaneous, Intramuscular
01

Overview

hMG + GnRH antagonist is a combination drug intervention used for controlled ovarian stimulation in women undergoing assisted reproductive techniques, such as intrauterine insemination (IUI). The combination consists of highly purified human menotropin (hMG-HP), marketed by Ferring Pharmaceuticals as Menopur, and a gonadotropin-releasing hormone (GnRH) antagonist. Menotropin provides both follicle-stimulating hormone (FSH) and luteinizing hormone (LH) activity to stimulate the growth and maturation of multiple ovarian follicles. The GnRH antagonist component acts by competitively binding to GnRH receptors in the pituitary gland, which rapidly suppresses the secretion of endogenous gonadotropins and prevents premature LH surges that could otherwise trigger untimely ovulation. This protocol is designed to improve clinical pregnancy rates by optimizing the timing of ovulation induction.

Brand names
Menopur
Other names
hMG + GnRH antagonisthuman menopausal gonadotropin + gonadotropin-releasing hormone antagonistmenotropin + GnRH antagonist
02

Targets

FSHR (Follicle-stimulating hormone receptor)LHCGR (Luteinizing hormone/choriogonadotropin receptor)GnRHR (Gonadotropin-releasing hormone receptor)

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