Ganirelix
Also known as: Ganirelix acetate, Orgalutran, Antagon
Ganirelix competitively blocks GnRH receptors on pituitary gonadotrophs, producing rapid, reversible suppression of LH and FSH secretion without an initial stimulatory flare.
- Drug class
- GnRH antagonist (synthetic decapeptide)
- Primary targets
- GnRH receptor, Pituitary gonadotroph, Luteinizing hormone (LH), Follicle-stimulating hormone (FSH)
- Dose reference
- Label dose of 0.25 mg subcutaneously once daily during the mid-to-late follicular phase until ovulation is triggered (a label figure, not a recommendation)
- Half-life
- About 12.8 hours after a single 0.25 mg dose; roughly 16.2 hours at steady state with daily dosing (label)
- Developer / origin
- N.V. Organon (Oss, the Netherlands)
- Reference year
- 1999
- Evidence score
- 4/5 - Approved, strong label and trial evidence within a narrow indication
Approved uses
- Inhibition of premature luteinizing hormone (LH) surges in women undergoing controlled ovarian stimulation as part of assisted reproductive technology (IVF)
Approved, strong label and trial evidence within a narrow indication
Ganirelix is FDA-approved (1999) with prescribing-information-backed pharmacology and phase III trial evidence supporting GnRH-antagonist protocols for preventing premature LH surges in controlled ovarian stimulation, though evidence is confined to this single IVF-adjunct indication.
Investigational compound with human randomized or phase 2/3 evidence.
Evidence basis
- FDA/DailyMed and Organon prescribing information document mechanism, pharmacokinetics (91% bioavailability, ~12.8 h half-life), 0.25 mg SC daily dosing and safety
- Phase III Fertility and Sterility trial compared ganirelix vs leuprolide acetate in controlled ovarian hyperstimulation
- Oberyé et al. phase I PK/PD studies established dose-proportional, rapidly reversible gonadotropin suppression
- ClinicalTrials.gov registered comparative trials (e.g., NCT00298025 vs cetrorelix)
Key references
- DailyMedGanirelix Acetate Injection prescribing information
- U.S. FDAAntagon (ganirelix acetate) Injection original approval label, 1999
- PubMed / Fertility and SterilityPharmacokinetic and pharmacodynamic characteristics of ganirelix, Part II
- Fertility and SterilityEfficacy and safety of ganirelix acetate versus leuprolide acetate in controlled ovarian hyperstimulation
How to read this entry
Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.
Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.
Ganirelix guides
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Peptide calculators
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Compare with related peptides
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