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LHRHa

Imperial College London · FDA-approved active Small molecule

LHRHa (Luteinizing Hormone-Releasing Hormone agonist) suppresses gonadal hormone production by desensitizing the pituitary gland to endogenous LHRH signaling.

LHRHa (Luteinizing Hormone-Releasing Hormone agonist) suppresses gonadal hormone production by desensitizing the pituitary gland to endogenous LHRH signaling. Used for Prostate cancer (hormone-sensitive), Breast cancer (hormone-sensitive), Endometriosis.

At a glance

Generic nameLHRHa
Also known asLupron®, leuprolide, Zoladex®, goserelin
SponsorImperial College London
Drug classLHRH agonist
TargetLHRH receptor (GnRH receptor)
ModalitySmall molecule
Therapeutic areaOncology
PhaseFDA-approved

Mechanism of action

LHRHa drugs bind to LHRH receptors on pituitary gonadotroph cells, initially causing a surge in luteinizing hormone (LH) and follicle-stimulating hormone (FSH), followed by receptor downregulation and sustained suppression of these hormones. This leads to reduced testosterone in males and estrogen in females, making these agents useful in hormone-dependent cancers and certain reproductive conditions.

Approved indications

Common side effects

Key clinical trials

Primary sources

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