Back to Peptide Library

Kisspeptin

KISS1-derived kisspeptin peptides: Kisspeptin-54 (Metastin) and Kisspeptin-10 (Metastin 45-54, YNWNSFGLRF-NH2)

Early-Stage ClinicalFDA Category 2Primary Endpoint Met

Access and compounding status raise extra safety and legal questions.

A natural brain signaling peptide that triggers the release of reproductive hormones -- studies in people show it rapidly raises the hormones that control fertility and sex hormone production. It is not FDA-approved and is not available through regular pharmacies due to limited safety data.

18 studiesUpdated 2026-03-10Subcutaneous · Intravenous

This entry is a cited research summary, not an established treatment reference. Dosing language is included as source context, not as medical instruction.

Clinical bottom lineMixed evidence

Kisspeptin has moderate clinical evidence but is not FDA-approved.

Access and compounding status raise extra safety and legal questions.

Safety Summary

The clearest reproducible human tolerability issue is tachyphylaxis: twice-daily SC kisspeptin-54 leads to marked desensitization of LH/FSH response within 2 weeks in women with hypothalamic amenorrhea PMID 19820030, mitigated by less frequent dosing (twice weekly maintained response over 8 weeks; PMID 26194072). Acute symptomatic safety reporting is limited in the filtered paper set. One 30-participant study in males reported no significant blood pressure change PMID 30046307. Review literature notes kisspeptin has been 'well-tolerated' with no serious adverse effects across multiple trials (PMID 24615662, PMID 26194072). However, FDA has identified potential significant safety risks including immunogenicity and peptide impurity concerns for compounded kisspeptin-10, and notes limited human safety data overall. In chronic animal studies, prolonged kisspeptin-54 administration (50 nmol/day SC for 13 days) caused testicular weight reduction and seminiferous tubule degeneration in rats via HPG axis desensitization PMID 35837314. Flushing and injection site reactions reported in clinical research context but not well-characterized in the filtered study set.

Clinical check-in

If real-world use or exposure is being considered, review potential interactions, contraindications, and monitoring needs with a licensed clinician rather than relying on summary copy alone.

See cited studies on this page (18)

Cited sources

Every claim on this page links to one of the 18 sources below. Identifiers are PubMed (PMID), ClinicalTrials.gov (NCT), or DOI; click through to the source of record before acting on a claim.

  1. 1PMID 21470997PubMed
  2. 2PMID 21632807PubMed
  3. 3PMID 21976724PubMed
  4. 4PMID 19820030PubMed
  5. 5PMID 30046307PubMed
  6. 6PMID 24615662PubMed
  7. 7PMID 26194072PubMed
  8. 8PMID 35837314PubMed
  9. 9PMID 29354093PubMed
  10. 10PMID 20501670PubMed
  11. 11PMID 19776272PubMed
  12. 12PMID 16339030PubMed
  13. 13PMID 16959837PubMed
  14. 14PMID 19934405PubMed
  15. 15PMID 41782211PubMed
  16. 16NCT03286517ClinicalTrials.gov
  17. 17NCT03771326ClinicalTrials.gov
  18. 18NCT03315325ClinicalTrials.gov