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triptorelin + progesterone
- Development stage
- Unknown
- Lead developer
- Assiut University
- Modality
- Peptides, Small Molecules
- Administration
- Subcutaneous, Vaginal
01
Overview
This combination therapy consists of the gonadotropin-releasing hormone (GnRH) agonist triptorelin and the steroid hormone progesterone, utilized as luteal phase support (LPS) in assisted reproductive technology (ART) cycles, such as in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Triptorelin acts as an agonist at the GnRH receptor in the pituitary gland, inducing a surge of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) that stimulates the corpora lutea to enhance endogenous steroid synthesis. Progesterone provides direct exogenous hormonal support to the endometrium, facilitating embryo implantation and maintaining early pregnancy. This specific investigational protocol typically involves a single mid-luteal dose of triptorelin (0.1 mg) administered subcutaneously on day 6 after oocyte pickup, in addition to standard transvaginal progesterone supplementation.
- Other names
- gonadotropins releasing hormone agonist + progesteroneGnRHa + progesteronetriptorelin and progesterone
02
Targets
PR (Progesterone receptor)GR (Glucocorticoid receptor)AR (Adrenergic receptors)GnRHR (Gonadotropin-releasing hormone receptor)MR (Mineralocorticoid receptor)
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