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

Cetrorelix

FDA approved · Rx

GnRH receptor antagonist

Also known as: Cetrotide, Cetrorelix Acetate, Cetrorelixum, SB-75, Cetrorelix (INN), SB 75

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. 140 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

Cetrorelix is a synthetic decapeptide that blocks gonadotropin-releasing hormone (GnRH) receptors in the pituitary gland. By blocking these receptors, it rapidly lowers the release of luteinizing hormone (LH) and follicle-stimulating hormone (FSH). It is sold under the brand name Cetrotide.

What the evidence shows

Automatic summaryHuman trials

Cetrorelix is FDA approved for preventing premature LH surges in women undergoing controlled ovarian stimulation as part of fertility treatment. It has a substantial research record, with about 140 registered human trials reaching Phase 4 and over 600 published papers, while uses outside its approved indication are less established.

Key facts

Molecular formula
C70H92ClN17O14
Molecular weight
1431 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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