Reproductive hormone
Human studies measure LH, FSH and testosterone responses; fertility and symptom benefits cannot be assumed.12
Reproductive hormone signaling peptide
Investigational; no FDA-approved kisspeptin-10 product identified.
10 residues · N → C4
Y–N–W–N–S–F–G–L–R–FC-terminal amide.
KP-10 is distinct from kisspeptin-54 and other analogs; molecular values exclude salt counterions.
Illustrative model using reported human data.
Five half-lives in this simplified model. This is not a prediction of when effects stop.
Kisspeptin immunoreactivity declined with mean half-lives of 3.8±0.3 minutes in men and 4.1±0.4 minutes in follicular/preovulatory women (SEM). The plotted value uses the male mean; this is not a subcutaneous absorption model.
Population: Healthy men and women
100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.
The cited 2005 Dhillo research concerns kisspeptin-54, not the kisspeptin-10 formulation in this profile.
Illustrative scenario using an unverified reference estimate.
Five half-lives in this estimated model. This is not a prediction of when effects stop.
Population: Not established by the reference estimate
Source’s stated attribution: Dhillo et al. 2005 J Clin Endocrinol Metab 90(12):6609-6615
Source’s reported peak time: 3 min. This has not been independently confirmed and is not used in the elimination curve.
100 × 2−time / half-life. Time zero is a reference level, not the moment of administration. Absorption, repeated dosing, metabolites and clinical effects are not modeled. Five half-lives leaves 3.125%, not zero. This curve cannot determine a dosing interval.
Scroll to compare all columns →
| Route | Dose | Frequency | Goal / evidence | Duration | References |
|---|---|---|---|---|---|
| IVIntravenous | 4 μg/kg/hour | Continuous infusion | Measure LH and testosterone responsesHealthy men; four in the prolonged-infusion groupHuman study | 22.5 hours | 1 |
Population Healthy men; four in the prolonged-infusion group Context Physiological hormone endpoints, not a validated fertility or libido treatment. | |||||
| SubQSubcutaneous infusion | 150 nmol/hour during infusion | 8 hours on, 16 hours off each day | Sustained gonadotropin secretionHealthy men; intermittent-infusion study armHuman study | 12 days | 6 |
Population Healthy men; intermittent-infusion study arm Context Research infusion regimen; not a bolus-injection or fertility-treatment recommendation. | |||||
| SubQ | 100-200 mcg | Single dose or 2-3x/week | Gonadotropin stimulationReference report | 2-4 weeks | 29 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims. Source tabs Injectable | |||||
| SubQSubQ (KP-54) | 0.4-1.0 nmol/kg (50-150 mcg) | As directed by physician | Fertility supportReference report | 2-4 weeks | 29 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims. Source tabs Injectable | |||||
| IVIV infusion | 1 nmol/kg/h | 75 min IV infusion (clinical) | Sexual functionReference report | 2-4 weeks | 29 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims. Source tabs Injectable | |||||
| SubQSubcutaneous | 0.3-10 nmol/kg | Variable by protocol | Research protocolsReference report | 2-4 weeks | 29 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims. Source route wording IV bolus or SubQ Source tabs Injectable | |||||
| IVIntravenous | 0.3-10 nmol/kg | Variable by protocol | Research protocolsReference report | 2-4 weeks | 29 |
Population Population not independently verified; see the reference and linked research. Context Reported in Pep-Pedia’s educational protocol table. Study attribution and applicability to this exact product are not independently established. Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims. Source route wording IV bolus or SubQ Source tabs Injectable | |||||
No protocols match these filters.
Study and label doses retain their study context. Reference reports are unvalidated practices, not personal treatment instructions. Ranges remain ranges; escalation stages are labeled.
Reported use periods and breaks. These do not establish a safe cycle or prove that breaks prevent tolerance.
Morning preferred for natural hormone rhythm
FDA identifies little or no safety information for proposed compounded routes.
3FDA flags possible immunogenicity and difficulties characterizing peptide impurities.
3Brief hormone studies in healthy adults do not establish reproductive, pregnancy or long-term safety.
2Repeated stimulation may desensitize responses; exact safe frequency unestablished. Heart disease warrants review.
Pelvic pain/bloating, chest pain, severe headache, mood changes, infection or precocious puberty signs.
Safety unestablished.
Not a complete safety screen. Discuss health decisions with a qualified clinician.
Check cautions and reported pairings. A compatibility claim does not establish that a combination is safe.
Upstream/downstream pathway relationship.29
Reference report · Pep-Pedia label: SynergisticClinical IVF comparison; not interchangeable self-use.29
Reference report · Evidence context: AlternativeFeedback-dependent; combination unvalidated.29
Reference report · Pep-Pedia label: CompatibleSex-steroid feedback matters.29
Reference report · Pep-Pedia label: CompatibleThese small physiology studies do not establish routine combination safety or interchangeable effects with kisspeptin-54.2
Research contextNo matching interactions. Try another name or filter.
Enter your peptide amount and container size. Get a volume and a simple measurement scale.
For dry powder, assuming negligible volume displacement. Use bacteriostatic water only if the formulation specifies it.
Amounts below are total blend mass. Ingredient amounts are listed separately.
| Pen units | Amount | Volume |
|---|
Enter an amount to calculate its volume and device setting.
The suggestion favors a simple 1, 2, or 5 × power-of-ten amount per unit, then the largest final volume that fits. It does not choose a dose or a biologically suitable concentration.
The water estimate applies only to dry powder and assumes negligible powder displacement. Final solution volume, specified diluent, solubility, stability, sterility, cartridge compatibility, and working fill limits must be established separately. No allowance is made for priming or transfer losses.
V2 measurement specification ↗Bacteriostatic water: formulation instructions ↗The human study used a controlled infusion preparation, not a universal research-vial recipe.5
For infusion, KP-10 was dissolved in saline containing 5% v/v Gelofusine. This study vehicle does not establish bacteriostatic-water compatibility or a home-use storage period.5
Reported handling information, not a validated formulation or instruction to prepare an injectable product.
The source reports BAC water and an optional acidification suggestion when dissolution is incomplete.
The source describes gentle mixing and avoiding vigorous shaking.
KP-10 and KP-54 are different compounds; their stability claims must not be interchanged.
Appearance and a purity certificate cannot establish sterility, identity, or suitability for injection.
Packaging examples, not a market survey. Approved and research products are not interchangeable.
Pep-Pedia reports these handling limits after mixing. They are not validated stability or sterility limits for your vial.
Storage depends on the formulation, diluent, container, and handling. Follow the specific product label or pharmacist’s instructions.
Device units measure volume. Concentration determines the amount in mg.
Documented 1-unit V2 models
Use the numbered dose window. Whole-unit settings only; confirm the specification for your exact model.
100 units = 1 mL
Read the printed unit scale. A small line may represent 0.5, 1, or 2 units depending on the syringe.
mL syringes and calibrated pipettes
Drops, sprays and other pen clicks need their own verified volume per increment. They have no universal conversion.
3 mL is cartridge capacity. It does not mean you must prepare or load 3 mL. The original vial and the pen cartridge are different containers. This reference compares measurement scales; it does not establish product or route compatibility.
Whether chronic use improves clinically meaningful fertility or sexual-health outcomes.1
6 distinct primary sources or abstracts checked. Evidence may concern a parent compound, individual blend ingredient, animal, or cell model; it does not necessarily establish a benefit for this exact product.
Evidence definitions →Source's blanket daily-use prohibition and 2–3× weekly limit are not validated universal protocols. Interaction labels are reference claims.
Kisspeptin-10 stimulates reproductive-hormone signaling in small human physiology studies. Changes in LH and testosterone are not proof of improved fertility, symptoms, or long-term health. Kisspeptin-54 is a different fragment.
Other names: KP-10 · KP10 · kisspeptin · metastin fragment · Kisspeptin-10 · KP-54
Investigational; no FDA-approved kisspeptin-10 product identified.
Human kisspeptin-10: Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2.4
10-54 amino acids · 1,213.42 Da (KP-10) / 6,087 Da (KP-54)
Kisspeptin-10: Tyr-Asn-Trp-Asn-Ser-Phe-Gly-Leu-Arg-Phe-NH2 | Kisspeptin-54: 54 amino acid C-terminal fragmentReference description; checked chemical identity takes precedence when available.29
KISS1R stimulation activates GnRH, then LH/FSH and gonadal hormones.29
In six healthy men, 1 μg/kg intravenously increased mean LH from 4.1 to 12.4 IU/L at 30 minutes. Four men receiving a prolonged infusion had higher LH and testosterone; these were hormone endpoints.
1A separate study with four or five people per group found hormone responses in men, but no gonadotropin rise in women during the follicular phase at the studied doses/routes.
2In healthy men, intermittent subcutaneous KP-10 infusion sustained LH and FSH stimulation for 12 days. Continuous infusion did not sustain the same gonadotropin response, showing that delivery pattern matters.
6Reproductive hormone research. Human studies measure LH, FSH and testosterone responses; fertility and symptom benefits cannot be assumed.12
Reproductive disorders. Research in hypogonadism, hypothalamic amenorrhea and IVF triggering; much clinical evidence concerns kisspeptin-54.29
Sexual desire. Human brain-response/arousal studies, not established routine therapy.29
Metabolism and body composition. Animal energy/glucose findings.29
PepPedia combines multiple kisspeptin fragments and discusses fertility and libido; its fragment-specific claims require careful reading.7
PepPedia's editorial protocol summary, not measured community consensus. Benefits, product identity, and safety are not independently verified; these reported practices are not recommendations. The cited row cannot establish a KP-10-specific regimen.
Added a randomized 2026 KP-10 infusion study. KP-54 bibliography and prior intravenous PK remain formulation specific.
AI-prepared summaries. Independent medical editorial review is pending.
Voluntary, unverified reports. These percentages do not measure effectiveness or safety.
Number of responses to this question: not disclosed.
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Number of responses to this question: not disclosed.
The source displays “903 responses” for this profile. This is not a confirmed participant count or a denominator for individual questions.
Original sources and review status. Open a reference to read its summary.
Small healthy-male cohorts showed acute LH stimulation and higher testosterone during continuous infusion; no fertility endpoint was established.
In six healthy men, 1 μg/kg intravenously increased mean LH from 4.1 to 12.4 IU/L at 30 minutes. Four men receiving a prolonged infusion had higher LH and testosterone; these were hormone endpoints.
Small cohorts showed context-dependent responses, including no gonadotropin change in follicular-phase women under the tested conditions.
A separate study with four or five people per group found hormone responses in men, but no gonadotropin rise in women during the follicular phase at the studied doses/routes.
Regulatory safety assessment.
Defines the human amidated decapeptide, formula and average molecular weight.
Full text of PMID 21976724: infusion vehicle and human immunoreactivity half-lives after stopping IV KP-10. Hormone responses vary by sex and cycle phase.
A randomized placebo-controlled study found sustained gonadotropin stimulation during intermittent subcutaneous KP-10 infusion for 12 days. Continuous infusion showed a different response pattern.
In healthy men, intermittent subcutaneous KP-10 infusion sustained LH and FSH stimulation for 12 days. Continuous infusion did not sustain the same gonadotropin response, showing that delivery pattern matters.
Additional research · Checked 2026-10-12
Secondary editorial account of discussed practices; not a clinical trial or representative survey.
Lists 5 mg and 10 mg configurations. Quantity examples only; vendor quality and suitability are not endorsed.
Pep-Pedia reports: Intranasal KP-54 stimulated gonadotropins in several human groups. The tested compound was kisspeptin-54, not kisspeptin-10.
Reported population / model
Humans
Reported study details
12.8 nmol/kg intranasal KP-54 · Healthy adults and HA patients
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The male HSDD trial reported brain-response changes and up to 56% greater penile tumescence; the specific kisspeptin isoform must be distinguished.
Reported population / model
Humans
Reported study details
32 men with HSDD · 1 nmol/kg/h IV infusion · 75 minutes · RCT
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Women showed changes in attraction-related brain processing and exploratory self-report measures; this does not establish routine treatment efficacy.
Reported population / model
Humans
Reported study details
32 women with HSDD · 1 nmol/kg/h IV infusion · 75 minutes · RCT
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The IVF report concerns KP-54, with 45% live births and no moderate/severe OHSS in the described study; KP-10 cannot inherit those results.
Reported population / model
Humans
Reported study details
Multiple doses tested · Subcutaneous KP-54 · Clinical trial
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: KP-10 constricted vessels and increased atherosclerotic lesions in mice; a receptor antagonist reversed the experimental effects.
Reported population / model
Human vessels and Apoe-/- mice
Reported study details
4-week KP-10 infusion · Ex vivo studies
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Female receptor-knockout mice became heavier despite eating less, with lower energy use and impaired glucose tolerance.
Reported population / model
Mice
Reported study details
Kiss1r knockout models · Long-term observation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Loss-of-function GPR54 variants were linked to pubertal failure and hypogonadotropic hypogonadism; genetic necessity does not define a treatment regimen.
Reported population / model
Humans
Reported study details
Genetic studies · Inactivating GPR54 mutations identified
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The male HSDD trial reported brain-response changes and up to 56% greater penile tumescence; the specific kisspeptin isoform must be distinguished.
Reported population / model
Humans
Reported study details
32 men with HSDD · 1 nmol/kg/h IV infusion · 75 minutes · RCT
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Women showed changes in attraction-related brain processing and exploratory self-report measures; this does not establish routine treatment efficacy.
Reported population / model
Humans
Reported study details
32 women with HSDD · 1 nmol/kg/h IV infusion · 75 minutes · RCT
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: The IVF report concerns KP-54, with 45% live births and no moderate/severe OHSS in the described study; KP-10 cannot inherit those results.
Reported population / model
Humans
Reported study details
Multiple doses tested · Subcutaneous KP-54 · Clinical trial
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Pep-Pedia reports: Loss-of-function GPR54 variants were linked to pubertal failure and hypogonadotropic hypogonadism; genetic necessity does not define a treatment regimen.
Reported population / model
Humans
Reported study details
Genetic studies · Inactivating GPR54 mutations identified
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Pep-Pedia reports: Female receptor-knockout mice became heavier despite eating less, with lower energy use and impaired glucose tolerance.
Reported population / model
Mice
Reported study details
Kiss1r knockout models · Long-term observation
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Pep-Pedia reports: KP-10 constricted vessels and increased atherosclerotic lesions in mice; a receptor antagonist reversed the experimental effects.
Reported population / model
Human vessels and Apoe-/- mice
Reported study details
4-week KP-10 infusion · Ex vivo studies
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Reference retained from Pep-Pedia’s bibliography; findings and bibliographic accuracy have not been independently verified.
Pep-Pedia bibliography · Checked 2026-10-12
Pep-Pedia reports: Intranasal KP-54 stimulated gonadotropins in several human groups. The tested compound was kisspeptin-54, not kisspeptin-10.
Reported population / model
Humans
Reported study details
12.8 nmol/kg intranasal KP-54 · Healthy adults and HA patients
Reported by Pep-Pedia; the linked publication, design, doses and result have not been independently verified here.
Read the Pep-Pedia report ↗Pep-Pedia reference card; original summary of its reported findings · Checked 2026-10-12
Lists a half-life of 28 min and a peak time of 3 min. Stated attribution: Dhillo et al. 2005 J Clin Endocrinol Metab 90(12):6609-6615. The cited 2005 Dhillo research concerns kisspeptin-54, not the kisspeptin-10 formulation in this profile. Five half-lives is not complete clearance, and the source’s “cleared” value is not used as a measured endpoint.
Secondary reference page checked; the underlying quantitative claim is not independently confirmed. · Checked 2026-10-12
Source page checked across available routes. Protocols, cycles, storage, mechanisms and pairing claims are secondary reports; checking the page does not independently validate those claims. Original concise summaries are used here.
Content coverage audit · Checked 2026-10-12