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Eligard (TM)
Eligard is a leuprolide acetate depot injection that suppresses luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to reduced testosterone production.
Eligard is a leuprolide acetate depot injection that suppresses luteinizing hormone (LH) and follicle-stimulating hormone (FSH), leading to reduced testosterone production. Used for Advanced prostate cancer, Prostate cancer requiring androgen deprivation therapy.
At a glance
| Generic name | Eligard (TM) |
|---|---|
| Sponsor | Chesapeake Urology Research Associates |
| Drug class | GnRH agonist |
| Target | GnRH receptor |
| Modality | Small molecule |
| Therapeutic area | Oncology |
| Phase | FDA-approved |
Mechanism of action
Leuprolide is a gonadotropin-releasing hormone (GnRH) agonist that initially stimulates the pituitary gland but with continuous exposure causes downregulation of GnRH receptors, resulting in sustained suppression of gonadal hormone secretion. This leads to castration-level testosterone suppression, which is the therapeutic goal in hormone-sensitive prostate cancer. Eligard is a sustained-release formulation designed to provide continuous drug delivery over weeks to months.
Approved indications
- Advanced prostate cancer
- Prostate cancer requiring androgen deprivation therapy
Common side effects
- Hot flashes
- Fatigue
- Erectile dysfunction
- Decreased libido
- Injection site reaction
- Gynecomastia
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Eligard (TM) CI brief — competitive landscape report
- Eligard (TM) updates RSS · CI watch RSS
- Chesapeake Urology Research Associates portfolio CI