Drug intelligence / Profile preview

medroxyprogesterone acetate + human menopausal gonadotropin

Development stage
Unknown
Lead developer
Pfizer
Modality
Small Molecules, Recombinant Proteins and Enzymes
Administration
Oral, Intramuscular, Subcutaneous
01

Overview

The combination of medroxyprogesterone acetate (MPA) and human menopausal gonadotropin (hMG) is the foundational regimen for the **Progestin-primed ovarian stimulation (PPOS)** protocol, pioneered by researchers at **Shanghai Ninth People's Hospital**. In this protocol, MPA is administered orally as a synthetic progestin to provide negative feedback on the hypothalamus-pituitary-ovarian axis, effectively suppressing premature luteinizing hormone (LH) surges during the follicular phase. Simultaneously, hMG (a purified extract containing both follicle-stimulating hormone and luteinizing hormone) is injected to stimulate the development of multiple ovarian follicles. This approach is particularly effective for patients with **polycystic ovary syndrome (PCOS)** and those undergoing 'freeze-all' IVF cycles, as the use of progestins prevents immediate embryo transfer by making the endometrium non-receptive, necessitating cryopreservation of embryos for future transfer.

Other names
MPA + hMGProgestin-primed ovarian stimulation protocolPPOS protocol
02

Targets

AR (Adrenergic receptors)FSHR (Follicle-stimulating hormone receptor)GABRR (GABA-A receptor subunit rho)GR (Glucocorticoid receptor)LHCGR (Luteinizing hormone/choriogonadotropin receptor)PR (Progesterone receptor)

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