Drug intelligence / Profile preview

Inadone (leuprorelin)

Development stage
Unknown
Modality
Peptides
Administration
Intramuscular, Subcutaneous
01

Overview

Inadone is a sustained-release microsphere formulation of leuprorelin acetate, a synthetic nonapeptide analog of naturally occurring gonadotropin-releasing hormone (GnRH). As a potent GnRH receptor agonist, leuprorelin initially stimulates the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH) from the pituitary gland. However, continuous administration leads to the downregulation and desensitization of GnRH receptors, resulting in a profound suppression of pituitary gonadotropins. This suppression leads to a significant reduction in serum testosterone levels in men (to castrate levels) and estradiol levels in women, making it effective for treating hormone-dependent conditions. Inadone is specifically developed as a long-acting injectable formulation to provide consistent therapeutic exposure over several months, primarily targeting prostate cancer and various endocrine disorders.

Brand names
Inadone
Other names
leuprorelin acetateleuprolide acetateleuprorelin acetate microspheres
02

Targets

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