Drug Database
LE

leuprolide (Lutrate)

✓ Approved

GP Pharm · GNRHR · Small Molecule

What is leuprolide?

leuprolide is a small molecule developed by GP Pharm. It is approved for therapeutic indications via injectable (others) or intramuscular (im) injection.

Drug Profile

Brand NamesLutrate
CompanyGP Pharm
Drug ClassSmall Molecule, Polypeptide
Molecular TargetGNRHR
RouteInjectable (Others), Intramuscular (IM) Injection
StatusApproved

Mechanism of Action

Molecular Targets

leuprolide acts on 1 molecular target:

GNRHRgonadotropin releasing hormone receptor (HH7, GRHR)
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Therapeutic Indications

leuprolide is developed for 1 unique indication across 1 therapeutic area.

Therapeutic AreaConditionPhase
Neoplasms benign, malignant and unspecified (incl cysts and polyps)Prostate cancer✓ Approved

Related Research Articles

PubMedGynecologic oncology reports2026-10-13

Persistently elevated estradiol after bilateral salpingo-oophorectomy in recurrent low-grade endometrial stromal sarcoma: a case report.

Moghaddam Ali Sanjari AS, Pastore Benjamin B, Turzio Maria Fernandez MF, McCash Samuel S et al.

Low-grade endometrial stromal sarcoma (LGESS) is a rare uterine mesenchymal neoplasm that frequently expresses estrogen and progesterone receptors. Endocrine therapy is a cornerstone of treatment for recurrent or metastatic LGESS. In premenopausal patients, bilateral salpingo-oophorectomy (BSO) is commonly performed to reduce endogenous estrogen production and would be expected to result in a postmenopausal hormonal profile. We report the case of a patient with recurrent, metastatic estrogen receptor (ER)/progesterone receptor (PR)-positive LGESS who had previously undergone BSO. Her disease initially responded to aromatase inhibitor therapy; however, she subsequently experienced pulmonary progression, including a large endobronchial metastasis requiring bronchoscopic cytoreduction. Despite pathologically confirmed BSO, further evaluation revealed a hormone profile more consistent with persistent premenopausal estrogen exposure. Given concern that ongoing estrogen exposure may have been contributing to progression of this hormone-sensitive malignancy, treatment was changed to combined leuprolide and letrozole. Three months after initiation of combined endocrine therapy, imaging demonstrated a partial response, which was confirmed at 6 months, accompanied by estradiol levels in the postmenopausal range. This case raises the possibility that surgical menopause may not always result in complete estrogen deprivation in LGESS. Potential explanations include assay limitations, undetectable residual gonadotropin-responsive steroidogenic tissue, peripheral aromatization, and tumor-associated estrogenic activity. Biochemical evaluation of estrogen status may be informative in select patients whose disease behavior appears discordant with presumed post-oophorectomy menopausal status.

PubMedIJU case reports2026-10-06

Prostatic Adenosquamous Carcinoma With a Minute Squamous Component in the Initial Biopsy and Early Liver Metastasis: A Case Report.

Tsubouchi Yohei Y, Naiki Taku T, Naiki-Ito Aya A, Unno Rei R et al.

We report a case of de novo prostatic adenosquamous carcinoma with a minute squamous component in the initial biopsy and early liver metastasis despite a marked prostate-specific antigen response. A 72-year-old man was diagnosed with locally advanced prostate cancer with nodal and multiple bone metastases. Prostate biopsy initially showed adenocarcinoma with a Gleason score of 4 + 5. After leuprolide and abiraterone plus radiotherapy, prostate-specific antigen decreased from 13.0 to 0.22 ng/mL; however, a liver metastasis developed. Re-evaluation of the prostate biopsy revealed minute squamous differentiation, and liver biopsy showed metastatic squamous cell carcinoma. Immunohistochemistry showed retained MLH1 and PMS2 expression with loss of MSH2 and MSH6 in both specimens. Genomic profiling showed microsatellite instability-high status. Repeat biopsy and molecular-pathological reassessment may be important when radiographic progression is discordant with prostate-specific antigen kinetics.

PubMedFrontiers in cell and developmental biology2026-09-15

Long-term testicular changes caused by the temporary suspension of puberty initiated at different stages of development.

Mancilla-Martínez Christian C, Contreras-García Itzel Jatziri IJ, Rojas-Castañeda Julio César JC, Landero-Huerta Daniel Adrian DA et al.

During puberty, secondary sexual characteristics develop alongside processes of testicular cell differentiation and maturation. Puberty suppression has been introduced to prevent the development of these physical changes in some individuals who request it, as is the case with gender dysphoria. However, not everyone continues with the treatment. Therefore, the objective of this study was to determine the testicular changes caused by the temporary suppression of puberty, initiated at different stages of development, in an experimental model. A total of 56 male rats were used, distributed equally into four study groups. A Control group, which received saline, and three experimental groups that received the GnRH analog (GnRHa), leuprolide acetate at 25 μg/kg/day. In the first of these groups, administration of the analog began during early puberty (LeuEP) on day postpartum (dpp) 25, equivalent to Tanner stages II-III in humans; in the second group, administration began during advanced puberty (LeuAP) at 35 dpp, equivalent to Tanner stages IV-V; and in the postpubertal group (LeuPP), administration began at 60 dpp. Half of the number of animals in each group were euthanized at 90 dpp, while the remaining animals had the GnRHa removed to allow recovery and were euthanized at 190 dpp. Testicular tissue was collected to assess histological and ultrastructural changes, as well as proteins that regulate the functional activity of Sertoli and Leydig cells. The LeuEP and LeuAP groups exhibited seminiferous tubules atrophy with peritubular cell hyperplasia, resulting in thickened tubular walls. They also showed Leydig cell hyperplasia with low immunoreactivity to the HSD17B3 enzyme, reduced immunoreactivity to androgen receptor proteins, and vimentin disorganization. These same groups showed partial recovery at 190 dpp, without reaching the values of the Control group. This may have been due to the persistence of thick tubular walls, possibly resulting from the dysfunction of Leydig cells and peritubular cells, which impeded the paracrine action of molecules necessary to maintain spermatogenesis. Furthermore, this was compounded by Sertoli cell dysfunction. Therefore, the temporary arrest of puberty initiated during puberty resulted in permanent testicular alterations, unlike in animals where GnRHa administration began postpubertally.

PubMedFrontiers in pharmacology2026-09-09

Comparison of Beiyi® and its reference product Enantone® as agonists of luteinizing hormone-releasing hormone against prostate cancer: a multicenter, randomized single-dose study.

Yi Yuyao Y, Shen Pengfei P, Zheng Tongsen T, Hou Ruigang R et al.

Leuprolide acetate is a potent agonist of luteinizing hormone-releasing hormone that has been licensed to treat prostate cancer. The microsphere formulation of leuprolide acetate called Beiyi®, developed in China, has shown favorable pharmacokinetics, pharmacodynamics and safety similar to those of the reference drug Enantone® in healthy individuals. The present study examined whether the two formulations are bioequivalent in men with prostate cancer. This multicenter, open-label study randomized 120 Chinese men with prostate cancer 1:1 to receive a single subcutaneous injection of Beiyi® or Enantone® (3.75 mg). The two groups were compared in terms of pharmacokinetics and safety. The ratio of the geometric means of the maximum serum concentration (Cmax) of Beiyi® and Enantone® was 98.34% (91.88%-105.25%); the ratio of the geometric means of the concentration-time curve from 7 to 28 days (AUC7-28) was 100.52% (88.17%-114.60%); and the ratio of the geometric means of the concentration-time curve from 0 to 28 days (AUC0-28) was 109.07% (98.54%-120.73%). The three 90% confidence intervals fell within the range of 80.00%-125.00%, indicating similar pharmacokinetics. The two drugs showed similar safety profiles, with no treatment-emergent adverse events leading to withdrawal or death. The two formulations of leuprolide acetate microspheres Beiyi® and Enantone® show similar pharmacokinetics and safety in Chinese men with prostate cancer. These results support the further clinical development of Beiyi® as a generic formulation of Enantone®. CTR20222654 on http://www.chinadrugtrials.org.cn/index.html.

PubMedCase reports in psychiatry2026-09-08

Breaking the Cycle: A Case of Delayed Diagnosis and Sustained Remission Following Definitive Surgical Treatment of Premenstrual Dysphoric Disorder (PMDD).

Deaton Daniel J DJ, Deaton Susannah L SL

Premenstrual dysphoric disorder (PMDD) is a hormone-sensitive mood disorder characterized by cyclical psychiatric and physical symptoms that impair functioning. Despite inclusion in DSM-5 and ICD-11, PMDD is frequently misdiagnosed or overlooked due to clinical unfamiliarity, lack of structured assessment, and systemic minimization of hormone-linked distress. Women routinely face delays in diagnosis and often only receive definitive treatment through self-advocacy. This report describes a 35-year-old cisgender female with treatment-resistant PMDD, whose symptoms began after menarche and worsened over two decades. Despite multiple psychiatric and medical encounters, her condition was misattributed to obesity, mood disorders, or trauma. After a diagnostic delay and multiple first and second-line treatment failures, a trial of leuprolide acetate confirmed a hormonal etiology of her symptoms, and she subsequently underwent total hysterectomy with bilateral salpingo-oophorectomy. Although she experienced a severe depressive episode in the immediate postoperative period, she has since remained in sustained symptom remission on an SSRI and estrogen replacement. This case demonstrates the need to recognize cyclic symptom patterns and potential hormonal etiology in treatment-resistant mood disorders.

PubMedThe Canadian journal of urology2026-09-02

Impact of leuprolide and goserelin on androgen suppression and adverse events in patients with prostate cancer.

Freitas Carla Simone Moreira CSM, Rocha-Silva Fabiana F, Marques-Silva Thaís Almeida TA, de Oliveira Ana Carolina Ribeiro ACR et al.

Androgen deprivation therapy (ADT) is widely employed in the management of advanced prostate cancer, with luteinizing hormone-releasing hormone (LHRH) agonists such as leuprolide and goserelin being common options. However, pharmacological and metabolic differences between these agents may affect the efficacy of hormonal suppression and adverse event profiles. This study compared the effects of leuprolide (22.5 and 45 mg) and goserelin (10.8 mg) on prostate-specific antigen (PSA) and testosterone reduction, as well as their metabolic and cardiovascular impacts and the influence of genetic variants on therapeutic response. A prospective, randomized, controlled study was conducted with 174 patients diagnosed with prostate cancer and treated with ADT for 12 months. Serum PSA and testosterone levels, lipid and glycemic profiles, and adverse events were monitored. Genetic analyses were performed to identify mutations in the TP53, BRCA1, BRCA2, and ATM genes. All treatment groups exhibited significant reductions in PSA and testosterone levels. Leuprolide 22.5 mg achieved the most pronounced PSA reduction, whereas goserelin 10.8 mg demonstrated greater variability in testosterone during the early months of therapy. Hot flashes were the most frequent adverse event, reported in 90% of patients treated with leuprolide 22.5 mg, while cardiovascular events were more prevalent in the goserelin 10.8 mg group. The TP53 gene was the most frequently altered (20.4%), followed by BRCA2 (7.4%) and ATM (6.5%), though these mutations did not significantly affect treatment response. ADT effectively achieves hormonal suppression in prostate cancer; however, differences between LHRH agonists influence clinical and metabolic outcomes. Leuprolide 22.5 mg showed superior PSA reduction but higher rates of vasomotor symptoms and weight gain, while goserelin 10.8 mg was associated with hormonal instability and cardiovascular risk. Genetic findings suggest that BRCA2 variants may affect lipid metabolism, reinforcing the need for personalized ADT strategies integrating metabolic and genetic profiles.

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