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Ultra-Long GnRH Agonists

University of Palermo · FDA-approved active Small molecule

Ultra-long GnRH agonists provide sustained suppression of gonadotropin-releasing hormone signaling, leading to prolonged inhibition of luteinizing hormone and follicle-stimulating hormone release.

Ultra-long GnRH agonists provide sustained suppression of gonadotropin-releasing hormone signaling, leading to prolonged inhibition of luteinizing hormone and follicle-stimulating hormone release. Used for Prostate cancer (androgen deprivation therapy), Endometriosis, Uterine fibroids.

At a glance

Generic nameUltra-Long GnRH Agonists
SponsorUniversity of Palermo
Drug classGnRH agonist
TargetGnRH receptor
ModalitySmall molecule
Therapeutic areaOncology; Endocrinology
PhaseFDA-approved

Mechanism of action

These agents bind to GnRH receptors and provide extended pharmacological activity through modified formulations or delivery systems, resulting in continuous suppression of the hypothalamic-pituitary-gonadal axis. This leads to sustained reduction in sex hormone production (testosterone and estrogen), with effects lasting weeks to months per dose. The ultra-long duration distinguishes them from conventional GnRH agonists by reducing dosing frequency and improving patient compliance.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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