El contenido de la evidencia se mantiene en inglés.

De un vistazo

ENTRY TYPE
investigational
IDENTITY
Sequence verified

No structure asset recorded

TOP EVIDENCE
Grade B — LH/FSH stimulation in healthy humans
MAJOR STATUS
Jurisdiction-specific — see status table
SPORT
Prohibited — as of 2026-08-06
VERIFIED
2026-08-06

Bottom line

Kisspeptin-54 (KP-54), originally named metastin, is the longest biologically active cleavage product of the KISS1 metastasis-suppressor gene. It acts as an agonist at KISS1R (GPR54) to stimulate GnRH and subsequent LH/FSH release. KP-54 is only — no FDA- or EMA-approved product was identified — with phase 1/2 trials in hypothalamic amenorrhea, hypogonadotropic hypogonadism, and as a potential fertility treatment. It has a longer plasma (28 min) than kisspeptin-10 (~4 min), making it the preferred isoform for most clinical studies.

Identity and composition

FieldVerified information
Preferred nameKisspeptin-54
Key aliasesKP-54; metastin; KISS1 (68-121); human metastin
Molecular/sequence identity54-amino-acid peptide; C-terminal decapeptide (residues 45-54) = kisspeptin-10
Modifications/formC-terminal amidation; full-length KISS1 product
Stable identifiersUniProt Q8NG95 (KISS1); IUPHAR/BPS ligand 1288
Identity caveatsHuman KP-54 sequence differs from other species, limiting translation. KP-54 and KP-10 are equipotent at KISS1R in vitro, but KP-54 has longer in vivo

Development and approval status

JurisdictionStatus and indicationProduct/sourceAs of
No jurisdiction; phase 1/2 clinical trials onlyResearch-grade peptide2026

Registered trials: NCT05633966 (KASPR, KP-10), NCT05896293 (KP-10), NCT04648969 (KP-10); intranasal KP-54 study (Abbara et al. 2025, EBioMedicine).

Status is multi-axis
Kisspeptin-54 authorization and sport-status profileFour medicine-authorization axes reproduce only documented status rows; sport status is shown separately.UNITED STATESSOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDEU/EEASOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDUNITED KINGDOMSOURCE ROW OMITTEDSEE AUDIT REASONSOURCE / AS OFNOT PRESENT / NOT RECORDEDOTHER DOCUMENTEDInvestigational; phase 1/2clinical trials onlySOURCE / AS OFROW 1 / 2026SPORT STATUS — SEPARATE FROM MEDICINE AUTHORIZATIONWADA: The 2026 List explicitly names kisspeptin and its agonist analogues under S2.2.1 astestosterone-stimulating peptides prohibited at all times in males. Kisspeptin stimulates
Authorization belongs to the named product, use, place, and date; sport status is independent.
Alternativa textual
UNITED STATES
No UNITED STATES row is present in the source status table
EU/EEA
No EU/EEA row is present in the source status table
UNITED KINGDOM
No UNITED KINGDOM row is present in the source status table
OTHER DOCUMENTED
No jurisdiction: Investigational; phase 1/2 clinical trials only

Sport status: WADA: The 2026 List explicitly names kisspeptin and its agonist analogues under S2.2.1 as testosterone-stimulating peptides prohibited at all times in males. Kisspeptin stimulates endogenous GnRH release but is not itself a GnRH analogue.

Mechanism and pharmacology

Full agonist at KISS1R on GnRH neurons, stimulating pulsatile GnRH release. KP-54 has a plasma of ~28 min in humans (vs. ~4 min for KP-10), and a volume of distribution of ~129 mL/kg. Continuous infusion can produce desensitisation, whereas pulsatile administration maintains responsiveness. KP-54 is equipotent with KP-10 in vitro but produces greater AUC for gonadotropins in vivo due to longer half-life.

Evidence by claim

Claim/indicationStageGradeBest human evidenceMain resultImportant limitations
LH/FSH stimulation in healthy humansPhase 1B, -controlled crossover (Dhirn et al. 2005)i.v. KP-54 (4 pmol/kg/min × 90 min) significantly increased LH, FSH, and testosteroneSmall n=6; acute only
Hypothalamic amenorrhea — LH pulsatiltyPhase 1/2CSingle-blind, dose-ranging (Jayasena 2013, PMID 24517142)KP-54 infusion increased LH pulses 3-fold vs. vehicle in HA womenSmall n=5; infusion only, no ovulation endpoint
Intranasal delivery feasibilityPhase 1C crossover (Abbara 2025)Intranasal KP-54 (12.8 nmol/kg) increased LH in healthy and HA subjectsIncludes KP-54 not KP-10; early stage
Niveles de evidencia
  • AGrado A: Establecido para un uso etiquetado específico
  • BGrado B: Evidencia humana moderada
  • CGrado C: Evidencia humana preliminar
  • DGrado D: Solo preclínico
  • EGrado E: Afirmación anecdótica/de marketing
  • XGrado X: La evidencia contradice o no respalda la afirmación
Más información sobre la clasificación de la evidencia
Claim-evidence profile
Kisspeptin-54 claim-evidence profileA: 0 claims; B: 1 claim; C: 2 claims; D: 0 claims; E: 0 claims; X: 0 claimsCONTRADICTORY / NON-SUPPORTIVEA — Established for a specific labeled useGrade A: Established for a specific labeled use — current approval plus adequate controlled trials and post-market context.0 claimsB — Moderate human evidenceGrade B: Moderate human evidence — multiple controlled studies or a strong pivotal study, but no current approval for the claim.1 claimLH/FSH stimulation in healthy humansC — Preliminary human evidenceGrade C: Preliminary human evidence — small, uncontrolled, surrogate-endpoint, or early-phase studies.2 claimsHypothalamic amenorrhea — LH pulsatiltyIntranasal delivery feasibilityD — Preclinical onlyGrade D: Preclinical only — in vitro or animal evidence with no adequate human efficacy evidence.0 claimsE — Anecdotal/marketing claimGrade E: Anecdotal/marketing claim — testimonials, extrapolation, or vendor claims without adequate scientific support.0 claimsX — Evidence contradicts or does not support the claimGrade X: Evidence contradicts or does not support the claim — adequate negative evidence, failed program, or claim inconsistent with the studied material.0 claims
This counts the page's claim rows; it does not average them into a score.
Alternativa textual

Text alternative for the claim-evidence diagram. Each grade is defined below:

AEstablished for a specific labeled use
0 claims
BModerate human evidence
1 claim: LH/FSH stimulation in healthy humans
CPreliminary human evidence
2 claims: Hypothalamic amenorrhea — LH pulsatilty; Intranasal delivery feasibility
DPreclinical only
0 claims
EAnecdotal/marketing claim
0 claims
XEvidence contradicts or does not support the claim
0 claims
OtherInvestigational; phase 1/2 clinical trials only

Key studies

StudyDesign/populationExposure studiedEndpoints and resultLimitations
Dhirn et al. (2005)DBPC crossover; healthy men (n=6)i.v. KP-54 4 pmol/kg/min × 90 min vs salineLH 10.8 vs 4.2 IU/L; FSH and T also significantly increasedn=6; short duration
Jayasena et al. (2013)Single-blind; women with HA (n=5)i.v. KP-54 infusion (0.01-1.0 nmol/kg/h × 8 h)Peak LH pulses 5.0/8h vs 1.6/8h (vehicle)Small n; not practical for chronic use
Abbara et al. (2025)DBPC crossover ; healthy men, women, HA patientsIntranasal KP-54 (3.2-25.6 nmol/kg)LH rise within 30-45 min; no AEsFirst intranasal data; small; device-dependent

Dose and administration evidence

Approved labeled regimen

Not applicable — not approved.

Studied regimens (not recommendations)

What is not established

No established or recommended human dose.

Safety

Human-study signals

  • Well-tolerated in all reported human studies.

  • No serious adverse events.

  • Mild subjective warmth, flushing at high doses.

  • No nausea or vasomotor symptoms reported with intranasal KP-54.

  • Desensitisation with continuous exposure; mitigated by pulsatile delivery.

Unknowns and product-quality risks

  • No chronic safety data (>2 weeks exposure).

  • No carcinogenicity or reproductive toxicity studies.

  • Online "kisspeptin-54" products are unregulated and may not be pure or correctly dosed.

Interactions and special populations

  • Not studied in pregnancy, lactation, children.

  • Baseline oestradiol levels affect LH response magnitude in women.

  • No studies with concurrent hormonal contraception.

Regulatory, compounding, and sport notes

  • Approval: No FDA-approved product or EMA-authorized medicine was identified; status elsewhere requires a current national-register check.

  • : The 2026 List explicitly names kisspeptin and its agonist analogues under S2.2.1 as testosterone-stimulating peptides prohibited at all times in males. Kisspeptin stimulates GnRH release but is not itself a GnRH analogue.

  • Compounding: No general exemption or lawful-compounding conclusion follows from status; applicable rules are product-, jurisdiction-, and fact-specific.

Evidence gaps

  • Chronic safety and desensitisation risk.

  • Efficacy for ovulation induction (phase 2/3 needed).

  • Optimal formulation and route.

  • Comparison with standard gonadotropin therapy.

Search notes

  • Databases and registries: PubMed, ClinicalTrials.gov, IUPHAR/BPS Guide to Pharmacology

  • Search terms: kisspeptin-54, KP-54, metastin, kisspeptin, human clinical trial

  • Last searched: 2026-08-06

  • Inclusion emphasis: Human clinical studies, registered trials

Sources

  1. Dhirn WS, et al. Kisspeptin-54 stimulates the HPG axis in human males. J Clin Endocrinol Metab. 2005;90(12):6609-15. PMID 16174713.

  2. Jayasena CN, et al. Increasing LH pulsatility in HA using KP-54 infusion. J Clin Endocrinol Metab. 2014;99(2):E243-51. PMID 24517142.

  3. Abbara A, et al. Intranasal KP-54 stimulates gonadotropin release. EBioMedicine. 2025. https://www.thelancet.com/journals/ebiom/article/PIIS2352-3964(25)00133-1/fulltext

  4. Chan YM, et al. Direct comparison of kisspeptin-10, -54, and GnRH. Hum Reprod. 2015;30(8):1849-56. PMID 26089302.

  5. IUPHAR/BPS Guide – kisspeptin-54 ligand ID 1288. https://www.guidetopharmacology.org/GRAC/LigandDisplayForward?ligandId=1288

  6. UniProt Q8NG95 (KISS1 precursor).

  7. WADA. 2026 Prohibited List. https://www.wada-ama.org/en/resources/world-anti-doping-program/prohibited-list

Voces de expertos

Lo que dicen los expertos

Los comentarios son opiniones y no forman parte de la revisión de la evidencia; la inclusión no implica respaldo.

No se encontraron comentarios de expertos verificados para este compuesto en las fuentes que acepta este atlas — literatura revisada por pares, comunicaciones universitarias, hospitalarias y de sociedades médicas, reguladores y periodismo científico con autoría nominal.

La ausencia de comentarios no es evidencia a favor ni en contra del compuesto.

Las afirmaciones de proveedores, clínicas y redes sociales están excluidas por política y no se contabilizan como comentarios.

Vídeos

Preguntas

What is kisspeptin-54?

Kisspeptin-54 (KP-54, originally named metastin) is the longest biologically active cleavage product of the KISS1 metastasis-suppressor gene. It acts as an endogenous agonist at KISS1R (GPR54) to stimulate GnRH and subsequent LH/FSH release.

Is kisspeptin-54 FDA-approved?

No. KP-54 is investigational only. No FDA-approved product or EMA-authorized medicine was identified as of August 2026. Phase 1/2 trials are exploring it for hypothalamic amenorrhea and as a potential fertility treatment.

What is the evidence quality for kisspeptin-54?

No established or recommended human dose. A double-blind placebo-controlled crossover study (n=6) found IV KP-54 significantly increased LH, FSH, and testosterone. A single-blind study in hypothalamic amenorrhea (n=5) showed a 3-fold increase in LH pulses. The evidence is Grade B for LH/FSH stimulation and Grade C for HA treatment due to small sample sizes.

What distinguishes kisspeptin-54 from kisspeptin-10?

KP-54 is the full-length 54-amino-acid product of KISS1, while KP-10 is a 10-mer C-terminal fragment. Both are equipotent in vitro, but KP-54 has a longer plasma half-life, producing greater gonadotropin AUC in vivo. KP-54 is the preferred isoform for most clinical studies.

What safety signals are reported for kisspeptin-54?

No established or recommended human dose. KP-54 is well-tolerated in all reported human studies with no serious adverse events. Mild subjective warmth and flushing occur at high doses. No nausea or vasomotor symptoms were reported with nasal KP-54. Desensitisation with continuous exposure is mitigated by pulsatile delivery. No chronic safety data beyond two weeks exposure exist.

Is kisspeptin-54 prohibited in sport?

Yes. The 2026 WADA Prohibited List names kisspeptin and its agonist analogues under S2.2.1 as testosterone-stimulating peptides prohibited at all times in males. KP-54 is an endogenous KISS1 product, not a GnRH analogue.

Actualizaciones de la investigación

Únase al atlas. Obtenga las actualizaciones de evidencia.

Reciba notas concisas cuando cambien la evidencia, el estado o los registros de origen de los péptidos.