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IndexedBuilt automatically from public databases on 2026-09-30. Not yet hand-reviewed by PLOBT.How this works →

Ganirelix

FDA approved · Rx

GnRH receptor antagonist

Also known as: Fyremadel, Ganirelix Acetate, Orgalutran, Ganirelixum, Antagon, Ganirelix (INN), CID 16134406

Evidence score
95/ 100
Strong evidence

Strong, human-grade evidence

  • Regulatory standing. FDA-approved prescription medicine
  • Human trials. Backed by controlled human studies
  • Registered human trials. 105 registered studies on ClinicalTrials.gov, most advanced Phase 4
  • 2 cited sources. Includes primary / regulatory sources

Computed with the same four public criteria as every profile. The human-evidence grade on an indexed profile is set automatically and may change when it is hand-reviewed. It is not a safety score, not a purity rating, and not medical advice, and not a claim that this compound treats, cures, or prevents any condition.

What it is

Ganirelix is a synthetic peptide that blocks gonadotropin-releasing hormone (GnRH) receptors in the pituitary gland. By blocking these receptors, it quickly lowers the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which can prevent an early LH surge during fertility treatment.

What the evidence shows

Automatic summaryHuman trials

Ganirelix is FDA approved for inhibiting premature LH surges in women undergoing controlled ovarian hyperstimulation as part of fertility treatment. It is supported by over 100 registered human trials, including Phase 4 studies, and a substantial published literature, while uses outside this indication are not established.

Key facts

Molecular formula
C80H113ClN18O13
Molecular weight
1570.3 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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