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Phase IIVendors pendingFacts verified · 2026-05-25

Kisspeptin

Also known as kisspeptin, metastin (45–54), kisspeptin-10, kp-10 · Wikipedia

Kisspeptin (KP-10, Kisspeptin-10, metastin 45-54) is the minimum bioactive C-terminal decapeptide of the KISS1 gene product. With sequence Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2, it is the endogenous ligand of the Gq-coupled GPCR KISS1R (formerly GPR54), the principal upstream regulator of the hypothalamic-pituitary-gonadal (HPG) axis. KP-10 triggers GnRH release from hypothalamic neurons, driving pulsatile LH and FSH secretion. Phase II clinical studies have evaluated it as an IVF oocyte-maturation trigger and in hypogonadotropic hypogonadism, hypothalamic amenorrhea, and hypoactive sexual desire disorder. It is not FDA-approved; KP-54 is the longer-half-life variant favored for IVF triggering.

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Mechanism of action

Kisspeptin-10 is the C-terminal decapeptide of KISS1 (metastin) and the minimum active fragment retaining full KISS1R agonism. KISS1R is densely expressed on hypothalamic GnRH neurons; KP-10 binding triggers Gq-mediated phospholipase-C activation, intracellular calcium rise, and depolarization-driven GnRH release.

Kisspeptin-10 is the C-terminal decapeptide of KISS1 (metastin) and the minimum active fragment retaining full KISS1R agonism. KISS1R is densely expressed on hypothalamic GnRH neurons; KP-10 binding triggers Gq-mediated phospholipase-C activation, intracellular calcium rise, and depolarization-driven GnRH release. Pulsatile GnRH then drives pituitary LH and FSH secretion; a single IV bolus produces a peak LH rise of ~45 IU/L at ~5 hours in healthy women (Abbara et al., PMID 36147569). Kisspeptin signaling is also detected in limbic and paralimbic structures; KP administration enhances limbic activation to sexual and bonding stimuli in functional MRI studies and modulates penile tumescence in men with hypoactive sexual desire disorder (Comninos et al., PMID 28112678; PMID 36287566; PMID 36735255). Loss-of-function KISS1R variants cause congenital hypogonadotropic hypogonadism.

Pharmacokinetic properties

Half-life

~4 minutes after IV bolus in humans (very short)

Routes

intravenous · subcutaneous

Bioavailability

IV infusion used in most rigorous human studies because of short half-life. SC dosing requires more frequent administration. Oral bioavailability negligible. Cheaper to manufacture than KP-54 due to shorter sequence.

Amino-acid sequence

Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2

Use & research dosing

Research framing only. Phase I/II human studies typically use intravenous bolus or infusion because of KP-10's very short plasma half-life (~4 minutes). Imperial College London trials have administered KP-10 at 0.1-3.0 nmol/kg as a single IV bolus for sexual-brain-processing and HPG-axis studies, and continuous IV infusions for amenorrhea reactivation. IVF triggering studies have generally favored KP-54 (kisspeptin-54) for its longer half-life (~28 minutes) rather than KP-10. There is no validated subcutaneous or oral protocol; gray-market SC dosing schedules have no controlled efficacy or safety data.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

Kisspeptin sits at the apex of the HPG axis and is one of the few peptides with credible human clinical work in both endocrine (IVF triggering, hypogonadotropic hypogonadism, hyperprolactinemic amenorrhea) and sexual-behavior (HSDD brain-imaging) indications, largely driven by the Imperial College London group (Dhillo, Comninos, Abbara). KP-10 is the shorter research variant; KP-54 is preferred for IVF triggering because of its longer half-life. Gray-market subcutaneous protocols for libido have no controlled efficacy or safety evidence and rely on extrapolation from IV-bolus human work.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • Not FDA-approved; investigational only - all clinical data are from academic Phase I/II trials
  • Pregnancy contraindicated outside controlled IVF triggering protocols - kisspeptin influences HPG axis
  • Hormone-sensitive cancers (breast, prostate, certain ovarian) - avoid pending long-term safety data
  • May trigger ovulation in women not desiring pregnancy
  • Very short plasma half-life (~4 min) makes consistent peripheral dosing difficult; SC bioavailability is uncharacterized
  • Reported transient headache, flushing, and injection-site reactions in trials
  • Theoretical risk of ovarian hyperstimulation when stacked with gonadotropin-stimulating protocols
  • Pediatric use contraindicated outside investigational settings
  • Drug interactions with hormonal contraceptives, GnRH analogs (leuprolide, triptorelin, gonadorelin), aromatase inhibitors not formally characterized
  • Vendor purity of gray-market peptide is not independently verified

Facts verified

2026-05-25

Confidence

medium

What this means

  • phase-II
  • imperial-college-program
  • kp-54-preferred-for-IVF

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