Eligard Information Center

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Expect more WITH ELIGARD®

Delivers proven, reliable testosterone suppression to low levels, with more flexibility and support for your patients and practice

Customizable dosing2,3

Multiple dosing options, including long-acting up to 6 months, to support customized treatment schedules for your patients

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Streamlined mixing & administration2,3

Convenient mixing system and flexible subcutaneous administration 


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Lowest cost among GnRH therapies4

Treatment cost is low, with no wholesale acquisition cost (WAC) increase in over a decade

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Comprehensive patient support from Tolmar

In-depth support is available for your patients and their care partners

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ELIGARD OFFERS MULTIPLE SUBCUTANEOUS INJECTION SITE OPTIONS FOR MORE FLEXIBILITY WITH EVERY ADMINISTRATION2
GnRH, gonadotropin-releasing hormone;
LHRH, luteinizing hormone–releasing hormone.
References: 1. Data on file. IQVIA data, Jan 2025-June 2026. Tolmar, Inc.; 2026. 2. ELIGARD (leuprolide acetate). Prescribing Information. Tolmar, Inc. 2026. 3. Prettyman J, Engel L, Boldt-Houle DM, Atkinson S, Wilt W. Personalizing treatment in the delivery of care by nurses to patients with prostate cancer. Urologic Nursing. 2019;39(2):83-99. 4. Data on file. Tolmar, Inc.; 2026.
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IMPORTANT SAFETY INFORMATION

ELIGARD® (leuprolide acetate) for injectable suspension is a gonadotropin releasing hormone (GnRH) agonist indicated for the treatment of advanced prostate cancer.
ELIGARD is contraindicated in patients with hypersensitivity to GnRH, GnRH agonists, or any of the components of ELIGARD. Anaphylactic reactions to synthetic GnRH or GnRH agonists have been reported in the literature. Transient increase in serum levels of testosterone during treatment may result in worsening of symptoms or onset of new signs and symptoms during the first few weeks of treatment, including bone pain, neuropathy, hematuria, bladder outlet obstruction, ureteral obstruction, or spinal cord compression. Monitor patients at risk closely and manage as appropriate.
Hyperglycemia and an increased risk of developing diabetes have been reported in men receiving GnRH agonists. Monitor blood glucose level and manage according to current clinical practice. Increased risk of myocardial infarction, sudden cardiac death and stroke has also been reported with use of GnRH agonists in men. Monitor for cardiovascular disease and manage according to current clinical practice. Androgen deprivation therapy may prolong the QT/QTc interval. Consider risks and benefits. Convulsions have been observed in patients taking leuprolide acetate with or without a history of predisposing factors. Manage convulsions according to current clinical practice. Severe cutaneous adverse reactions (SCARs), including Stevens-Johnson syndrome/toxic epidermal necrolysis, and erythema multiforme, occurred in patients receiving ELIGARD. Monitor for and advise patients of the signs and symptoms of SCARs. May cause fetal harm.
ELIGARD may impair fertility in males of reproductive potential.
The most common injection site adverse events are transient burning and stinging, pain, bruising, and erythema. The most common systemic adverse events include mild to severe hot flashes/sweats, malaise and fatigue, weakness, myalgia, dizziness, clamminess, testicular atrophy, and gynecomastia. As with other GnRH agonists, other adverse reactions, including decreased bone density and rare cases of pituitary apoplexy have been reported.

Please see full Prescribing Information for ELIGARD.

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