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
| Claim | Evidence | Notes |
|---|---|---|
| Advanced prostate cancer | Approved use | FDA and TGA approved; as effective as diethylstilbestrol with fewer side effects in a 1984 randomised trial. |
| Endometriosis pain and lesions | Approved use | Lupron 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 surgery | Approved use | Label indication with iron therapy. |
| Central precocious puberty in children | Approved use | Lupron Depot-Ped label indication. |
Side effects
| Effect | How often | Notes |
|---|---|---|
| Hot flushes and sweats | Common | Over 10% in prostate cancer and gynaecology trials. |
| Headache, depression or mood changes, reduced libido, dizziness | Common | Over 10% in gynaecology label trials. |
| Injection site reactions, general pain, fatigue, oedema | Common | Over 10% in some prostate cancer depot trials. |
| Testicular shrinkage and erectile problems | Common | Expected effect of testosterone suppression. |
| Loss of bone mineral density Serious | Common | Limits treatment length in women; add back therapy reduces loss. |
| Tumour flare in the first weeks Serious | Common | Testosterone rises about 50% initially; can worsen bone pain, urinary obstruction or spinal cord compression. |
| Diabetes, raised lipids and fatty liver Serious | Frequency unknown | Metabolic syndrome warning on the label. |
| Heart attack, sudden cardiac death, stroke and QT prolongation Serious | Frequency unknown | Increased risk reported with GnRH analogues in men. |
| Convulsions Serious | Rare | Reported with or without predisposing factors. |
| Severe skin reactions (SJS/TEN, DRESS) Serious | Rare | Label warning; stop treatment if suspected. |
| Anaphylaxis Serious | Rare | Reported 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
- DailyMed: Lupron Depot (leuprolide acetate) label, prostate cancer
- DailyMed: Lupron Depot 3.75 mg label, endometriosis and fibroids
- DailyMed: Lupron Depot-Ped label
- PubMed: Leuprolide versus diethylstilbestrol for metastatic prostate cancer (1984)
- Drugs@FDA: Lupron NDA 019010
- TGA ARTG search: leuprorelin
- 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.