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SHR7280 is an oral, non-peptide small molecule gonadotropin-releasing hormone (GnRH) antagonist developed by Jiangsu Hengrui Medicine. It acts by competitively binding to GnRH receptors in the anterior pituitary gland, thereby inhibiting GnRH receptor signaling and suppressing the secretion of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). This leads to a reduction in sex hormone levels such as estrogen and progesterone. SHR7280 is being investigated for the treatment of sex hormone-dependent disorders including endometriosis, menorrhagia with uterine fibroids, female infertility, and prostate cancer.
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