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

Leuprolide

FDA approved · Rx

GnRH receptor agonist

Also known as: Lupron, Eligard, Fensolvi, leuprorelin, Lupron Depot, Camcevi, Vabrinty, Leuprolide Acetate, Leuprorelin, Leuprorelina

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. 521 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

Leuprolide, also called leuprorelin, is a synthetic peptide analog of gonadotropin-releasing hormone (GnRH). It first stimulates and then, with continued exposure, suppresses the pituitary's release of LH and FSH, which lowers testosterone and estrogen production.

What the evidence shows

Automatic summaryHuman trials

Leuprolide is FDA-approved, under brands such as Lupron Depot, Eligard, Camcevi, and Fensolvi, for conditions including advanced prostate cancer, endometriosis, uterine fibroids, and central precocious puberty, with specific indications varying by product. It is supported by a large body of evidence, with about 520 registered human trials reaching Phase 4 and over 2,400 published papers.

Key facts

Molecular formula
C59H84N16O12
Molecular weight
1209.4 g/mol
FDA approval
Confirmed on openFDA

Registered human trials

Published literature

Sources

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