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LhRH-antagonist

Turku University Hospital · FDA-approved active Small molecule

LhRH antagonists block luteinizing hormone-releasing hormone receptors to suppress gonadotropin secretion and reduce sex hormone production.

LhRH antagonists block luteinizing hormone-releasing hormone receptors to suppress gonadotropin secretion and reduce sex hormone production. Used for Prostate cancer (hormone-sensitive), Endometriosis, Uterine fibroids.

At a glance

Generic nameLhRH-antagonist
Also known asDegarelix 120 MG
SponsorTurku University Hospital
Drug classGnRH/LhRH antagonist
TargetGnRH receptor (LhRH receptor)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

LhRH antagonists competitively bind to GnRH receptors in the pituitary gland, immediately blocking the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). This leads to rapid suppression of testosterone in males and estrogen in females, without the initial testosterone surge seen with GnRH agonists. The mechanism is used therapeutically to suppress sex hormone-dependent conditions.

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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