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Leuprorelin Acetate Depot 3M

Takeda · FDA-approved active Small molecule

Leuprorelin acetate is a GnRH agonist that suppresses luteinizing hormone and follicle-stimulating hormone, leading to decreased testosterone and estrogen production.

Leuprorelin acetate is a GnRH agonist that suppresses luteinizing hormone and follicle-stimulating hormone, leading to reduced testosterone and estrogen production. Used for Advanced prostate cancer, Hormone receptor-positive breast cancer (premenopausal women), Endometriosis.

At a glance

Generic nameLeuprorelin Acetate Depot 3M
Also known asLeuprolide acetate Depot 3M
SponsorTakeda
Drug classGnRH agonist
TargetGnRH receptor
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

Leuprorelin works by binding to GnRH receptors in the pituitary gland, initially causing a surge in LH and FSH (flare effect), followed by sustained suppression of these hormones through receptor desensitization. This results in castration-level testosterone suppression in males and estrogen suppression in females, making it effective for hormone-dependent conditions. The depot formulation provides sustained release over 3 months.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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