Library / Hormonal

Leuprorelin

Also known as Leuprolide, Lucrin, Eligard, Lupron

Approved medicine

Gonadotrophin releasing hormone agonist nonapeptide that suppresses sex hormones with ongoing use. Approved for hormone dependent cancers and gynaecological conditions, and used in some IVF protocols.

Prescription medicine. Only a prescriber can decide whether a medicine suits you and at what dose. This page is information, not a recommendation.

Background

Synthetic nonapeptide analogue of GnRH (des-Gly10, D-Leu6 LHRH ethylamide) developed in Japan by Takeda in the 1970s. Daily injections were first FDA approved in 1985 for prostate cancer (Lupron), followed by long acting depots.

How it is thought to work

A potent GnRH receptor agonist. It first causes a surge in LH, FSH and sex hormones (a 'flare'), then with continued exposure the pituitary shuts down, reducing testosterone or oestrogen to very low levels. This is reversible after stopping.

What is claimed, and the evidence

ClaimEvidenceNotes
Advanced prostate cancerApproved useFDA and TGA approved; as effective as diethylstilbestrol with fewer side effects in a 1984 randomised trial.
Endometriosis pain and lesionsApproved useLupron Depot 3.75 mg and 11.25 mg label indication, limited to 12 months total with add back therapy because of bone loss.
Fibroids with anaemia before surgeryApproved useLabel indication with iron therapy.
Central precocious puberty in childrenApproved useLupron Depot-Ped label indication.

Side effects

EffectHow oftenNotes
Hot flushes and sweatsCommonOver 10% in prostate cancer and gynaecology trials.
Headache, depression or mood changes, reduced libido, dizzinessCommonOver 10% in gynaecology label trials.
Injection site reactions, general pain, fatigue, oedemaCommonOver 10% in some prostate cancer depot trials.
Testicular shrinkage and erectile problemsCommonExpected effect of testosterone suppression.
Loss of bone mineral density
Serious
CommonLimits treatment length in women; add back therapy reduces loss.
Tumour flare in the first weeks
Serious
CommonTestosterone rises about 50% initially; can worsen bone pain, urinary obstruction or spinal cord compression.
Diabetes, raised lipids and fatty liver
Serious
Frequency unknownMetabolic syndrome warning on the label.
Heart attack, sudden cardiac death, stroke and QT prolongation
Serious
Frequency unknownIncreased risk reported with GnRH analogues in men.
Convulsions
Serious
RareReported with or without predisposing factors.
Severe skin reactions (SJS/TEN, DRESS)
Serious
RareLabel warning; stop treatment if suspected.
Anaphylaxis
Serious
RareReported with GnRH agonists.

Warnings

  • May cause fetal harm; pregnancy must be excluded and non hormonal contraception used.
  • Initial hormone flare can transiently worsen cancer or endometriosis symptoms.
  • Long term use causes bone loss and raises metabolic and cardiovascular risks.

Regulatory status

Australia
Approved (ARTG, multiple products).
United States
FDA approved (Lupron and other products) for prostate cancer, endometriosis, fibroids and central precocious puberty.

Sources

  1. DailyMed: Lupron Depot (leuprolide acetate) label, prostate cancer
  2. DailyMed: Lupron Depot 3.75 mg label, endometriosis and fibroids
  3. DailyMed: Lupron Depot-Ped label
  4. PubMed: Leuprolide versus diethylstilbestrol for metastatic prostate cancer (1984)
  5. Drugs@FDA: Lupron NDA 019010
  6. TGA ARTG search: leuprorelin
  7. Drugs@FDA: Lupron Depot-Ped (leuprolide)

Also in Hormonal

From the VialOwl library, reviewed 26 September 2026. For education and general information. It is not medical advice and not a recommendation to use Leuprorelin.