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

Goserelin

FDA approved · Rx

GnRH agonist peptide

Also known as: Zoladex, Decapeptide I, Goserelina, Gosereline, Goserelinum, ICI-118630, ICI 118630, ICI 118,630

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. 417 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

Goserelin is a synthetic peptide analog of gonadotropin-releasing hormone (GnRH), sold under the brand name Zoladex. After an initial surge, continued exposure desensitizes GnRH receptors in the pituitary, which lowers production of LH and FSH and in turn reduces testosterone and estrogen levels.

What the evidence shows

Automatic summaryHuman trials

Goserelin is FDA-approved as a prescription drug, approved for conditions including advanced prostate cancer, certain breast cancers, endometriosis, and endometrial thinning before surgery. It has a large body of human evidence, with over 400 registered trials reaching Phase 4 and more than 1,200 published papers.

Key facts

Molecular formula
C59H84N18O14
Molecular weight
1269.4 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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