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GnRH antagonist-Cetrorelix

University of Edinburgh · FDA-approved active Small molecule

Cetrorelix blocks gonadotropin-releasing hormone (GnRH) receptors to suppress luteinizing hormone and follicle-stimulating hormone secretion.

Cetrorelix blocks gonadotropin-releasing hormone (GnRH) receptors to suppress luteinizing hormone and follicle-stimulating hormone secretion. Used for Controlled ovarian hyperstimulation in assisted reproductive technology (ART), Prostate cancer (advanced), Endometriosis.

At a glance

Generic nameGnRH antagonist-Cetrorelix
Also known asCetrotide
SponsorUniversity of Edinburgh
Drug classGnRH antagonist
TargetGnRH receptor
ModalitySmall molecule
Therapeutic areaReproductive Medicine / Endocrinology
PhaseFDA-approved

Mechanism of action

Cetrorelix is a GnRH antagonist that competitively binds to GnRH receptors on pituitary gonadotroph cells, rapidly suppressing the release of LH and FSH without an initial flare effect. This leads to immediate inhibition of sex hormone production (testosterone and estrogen), making it useful in reproductive medicine and hormone-sensitive 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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