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Phase IIVendors pendingFacts verified · 2026-05-25

Kisspeptin-54

Also known as metastin, kiss-1 (68–121) amide, kp-54 · Wikipedia

Kisspeptin-54 (KP-54, metastin) is the full-length 54-amino-acid C-terminally amidated cleavage product of the KISS1 prepropeptide and an agonist at the KISS1R / GPR54 receptor. It is the longer-acting member of the kisspeptin family and the form most rigorously studied in human reproductive endocrinology, particularly as an IVF oocyte-maturation trigger by the Imperial College London group (Dhillo, Abbara, Comninos). It triggers hypothalamic GnRH release, driving LH/FSH secretion and gonadal steroidogenesis, and is being explored as a more physiologic alternative to hCG and GnRH agonist triggers, with apparently lower OHSS risk.

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Mechanism of action

Kisspeptin-54 is the full-length, C-terminally amidated 54-amino-acid product of the KISS1 prepropeptide. Like KP-10 it binds KISS1R (GPR54), a Gq-coupled GPCR on hypothalamic GnRH neurons, but the longer sequence confers higher in-vivo potency and a substantially longer plasma half-life (~28 min SC vs ~4 min for KP-10 IV).

Kisspeptin-54 is the full-length, C-terminally amidated 54-amino-acid product of the KISS1 prepropeptide. Like KP-10 it binds KISS1R (GPR54), a Gq-coupled GPCR on hypothalamic GnRH neurons, but the longer sequence confers higher in-vivo potency and a substantially longer plasma half-life (~28 min SC vs ~4 min for KP-10 IV). KISS1R activation triggers pulsatile GnRH release, driving LH and FSH secretion from the pituitary and downstream gonadal steroidogenesis and oocyte maturation. In IVF, Phase 2 trials by Abbara, Jayasena, and Dhillo (Imperial College London) demonstrated that KP-54 can trigger oocyte maturation in women at high risk of OHSS with reduced incidence of severe OHSS versus hCG (PubMed 26192876).

Pharmacokinetic properties

Half-life

~28 minutes after subcutaneous dosing in humans (vs ~4 min for KP-10 IV)

Routes

subcutaneous · intravenous

Bioavailability

Longer half-life makes SC dosing more practical than KP-10. Oral bioavailability negligible. More expensive to synthesize than KP-10.

Amino-acid sequence

(54 aa) Metastin (1-54), C-terminally amidated

Use & research dosing

No FDA-approved dose. In published clinical research, 1.6-12.8 nmol/kg subcutaneous single bolus has been used as an IVF oocyte-maturation trigger, and 0.1-3.0 nmol/kg as an IV bolus in HPG-axis studies. A second-dose 10 h after the first improves oocyte yield in high-OHSS-risk women. Self-experimentation outside fertility-research contexts is uncommon because of cost and limited vendor supply. Research framing only.

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

Editorial perspective

Key distinction from KP-10: same gene product, longer chain, roughly 7x longer plasma half-life, more potent in vivo per molecule. The most rigorous human HPG-axis and IVF data exist for KP-54 rather than KP-10. Imperial College London (Dhillo, Abbara, Comninos, Jayasena) has driven the IVF oocyte-maturation trigger program through Phase 2 trials in high-OHSS-risk women; clinical development beyond Phase 2 has not produced a registered product to date.

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

Cautions & contraindications

Before researching this compound, note:

  • Not FDA-approved for any indication
  • HPG-axis stimulation inappropriate in hormone-sensitive cancers (breast, prostate, endometrial)
  • Pregnancy and lactation safety unknown outside fertility-trigger trials
  • Risk of OHSS appears reduced versus hCG but is not zero
  • May interfere with hormonal contraception and other HPG-active medications
  • Limited long-term safety data outside Phase 2 trial cohorts
  • IVF use should be in a controlled clinical setting with monitoring
  • Vendor-grade material lacks pharmaceutical sterility and identity assurance

Facts verified

2026-05-25

Confidence

medium

What this means

  • Phase 2 IVF trials only; no Phase 3 / regulatory approval
  • off-label use outside controlled IVF context lacks safety data

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