LH response
Rapid after administration, and brief for kisspeptin-10.

Protocol / Research Dosing Guide
A source-gated Kisspeptin-10 reference that separates published kisspeptin-54 trial protocols from the shorter kisspeptin-10 form sold for research use.
Kisspeptin-10 is the short form of the kisspeptin signal and acts upstream of GnRH to trigger LH and FSH release. It acts fast and clears fast: after intravenous dosing its blood half-life is roughly four minutes. Most human trial data uses the longer kisspeptin-54 form, and those trial doses are given in nmol/kg, so they do not convert neatly to a microgram amount.
Why researchers care
GnRH pulse generation, LH and FSH response, reproductive-axis research
Class
Decapeptide fragment of kisspeptin acting at the KISS1R (GPR54) receptor
Route reported
Subcutaneous in research-use planning; intravenous in several trials
Cycle length
Short pulse cycles reported because of desensitization
Regulatory status
Not FDA approved
The supplied source reports research-context kisspeptin-10 ranges of 50–100 mcg once daily subcutaneously, 100–200 mcg once daily, or 100 mcg twice daily, and separately lists kisspeptin-54 trial protocols in nmol/kg.
| Phase or study | Amount | Frequency / evidence |
|---|---|---|
| Low-dose pulse | 50–100 mcg once daily subcutaneously | Research-context reported |
| Standard pulse | 100–200 mcg once daily subcutaneously | Research-context reported |
| Split dose | 100 mcg twice daily subcutaneously | Research-context reported |
| Short pulse cycle | 2–4 weeks active, 2–4 weeks off | Reported cycle structure |
| Standard cycle | 4–6 weeks active, 4 weeks off | Reported cycle structure |
Continuous exposure can make the LH signal fade, an effect called tachyphylaxis or desensitization. That is why reported structures use short pulses rather than nonstop exposure.
Neutral research-material planning only. This does not establish an appropriate amount or route.
Research planning item
Exact labeled research vial
Research planning item
Bacteriostatic water at a measured volume
Research planning item
U-100 insulin syringes, 0.3 mL barrel for accurate small draws
Research planning item
Alcohol prep swabs
Research planning item
Sharps container
Research planning item
Refrigeration for the prepared vial
Research planning item
Written concentration label
Concentration
5 mg/mL
Draw volume
0.02 mL
U-100 units
2
Mathematical draws
100
Arithmetic only. The entered amount is not a recommendation and does not establish suitability.
Not established. Reported low-dose planning often describes administration before sleep.
Both appear in reported research-context ranges.
Avoided in reported practice because the LH response fades with sustained exposure.
No validated procedure exists.
| Format | What is reported | Evidence limit |
|---|---|---|
| Subcutaneous kisspeptin-10 | The form most research-use suppliers stock | Short signal window |
| Subcutaneous kisspeptin-54 | Used in IVF trigger and desire-related trials | Different molecule and duration |
| Intravenous infusion | Used in several published trials | Not a research-community route |
Routes and amounts are not interchangeable unless a verified study explicitly establishes a conversion.
| Measure | Finding | Evidence limit |
|---|---|---|
| Kisspeptin-10 (intravenous) | About 4 minutes | Published |
| Kisspeptin-54 (subcutaneous) | About 28 minutes, with LH elevated for several hours | Published |
| Why pulses are short | The LH and FSH signal is brief even when a subcutaneous route stretches it slightly | Reported rationale |
| Desensitization | Sustained exposure reduces the response over time | Observed in a chronic twice-weekly trial |
| Route | Amount | Frequency | Source | Human validation |
|---|---|---|---|---|
| Subcutaneous (K-10) | 50–100 mcg | Once daily | Research-context report | No |
| Subcutaneous (K-10) | 100–200 mcg | Once daily | Research-context report | No |
| Subcutaneous (K-10) | 100 mcg | Twice daily | Research-context report | No |
| Subcutaneous (K-54) | 1.6–12.8 nmol/kg single bolus | IVF trigger studies | Clinical trial | No |
| Subcutaneous (K-54) | 6.4 nmol/kg | Twice weekly | Hypothalamic amenorrhea trial | No |
| Intravenous (K-54) | 1 nmol/kg/hour | 75-minute infusion | Clinical trial | No |
Published study values describe those studies. Community-reported values are not validated dosing recommendations.
Concentration: 5 mg/mL
| Entered amount | Volume | U-100 units |
|---|---|---|
| 0.1 mg | 0.02 mL | 2 units |
| 0.2 mg | 0.04 mL | 4 units |
| 0.3 mg | 0.06 mL | 6 units |
Reconstitution does not establish identity, purity, sterility, stability, or an appropriate amount.
Kisspeptin binds KISS1R, also called GPR54, on GnRH neurons.
Current status · verified September 16, 2026
Not FDA approved
This is an evidence-gap and precaution list, not an approved prescribing label.
Pregnancy or breastfeeding
No safety data outside supervised trials
Hormone-sensitive conditions
Reproductive-axis stimulation is not evaluated in this setting
Children or adolescents
Puberty-axis effects are not characterized
Undiagnosed endocrine or fertility problems
Requires clinical diagnosis before any hormone intervention
Continuous unsupervised use
Desensitization and unmonitored hormone change
Important limitation: No controlled incidence data.
Important limitation: Generally transient.
Important limitation: No controlled incidence data.
Important limitation: Sustained exposure reduces response.
Important limitation: No interaction studies for research-use protocols.
Important limitation: No follow-up evidence.
Rapid after administration, and brief for kisspeptin-10.
LH peaked at about five hours and returned to pre-trigger levels by 12 to 14 hours.
Two to six weeks active with a matching off period.
No validated monitoring schedule exists outside trials.
| Claim | Evidence level | What research shows | Important limitation |
|---|---|---|---|
| LH and FSH release | Demonstrated in human studies | Level 3 | Acute signal, not an outcome |
| IVF trigger use | Trial evidence with kisspeptin-54 | Level 3 | Different molecule |
| Testosterone increase | Conditional | Depends on testicular responsiveness | Not a validated protocol |
| Desire-related endpoints | Trial research with kisspeptin-54 | Level 3 | Not transferable to kisspeptin-10 |
Follow the product label; keep cool, dry and out of light.
Refrigerate and protect from light.
Repeated freeze-thaw cycles are avoided for peptide solutions.
Cloudiness, discoloration or particles mean the solution should not be used.
They depend on body weight. For example, 6.4 nmol/kg of kisspeptin-54 is about 2.85 mg for a 70 kg subject.
That pattern matches reported desensitization from sustained exposure.
At 5 mg/mL, 100 mcg is only 2 units; use a 0.3 mL syringe for a readable draw.
Stop and seek qualified product guidance.
Seek licensed clinical review.
| Compound | Class or mechanism | Evidence | FDA status |
|---|---|---|---|
| Kisspeptin-10 | Short decapeptide form | About 4 minute intravenous half-life | Not approved |
| Kisspeptin-54 | Full-length form used in trials | About 28 minute subcutaneous half-life | Not approved |
| HCG | Acts directly at the LH receptor | Downstream of kisspeptin | Approved in defined indications |
A decapeptide that acts at KISS1R on GnRH neurons to trigger LH and FSH release.
No.
About four minutes after intravenous dosing.
It lasts longer, with about a 28 minute subcutaneous half-life and hours of raised LH.
Not neatly. The conversion depends on body weight and on which form is used.
The fading LH response seen with continuous exposure.
5 mg/mL, so 100 mcg is 2 units on a U-100 syringe.
Human data shows LH can rise; a testosterone rise depends on the testes responding.
No. Reported two-to-six week structures are research-context planning, not trial protocols.
At 100 mcg per administration it covers roughly 100 planned draws before losses.
Concentration and volume arithmetic only.
Coverage source
Supplied coverage source for research-context ranges, cycle structures and vial arithmetic.
Open direct sourceClinical trial
Phase 2 trial work reporting nmol/kg bolus dosing and LH response windows.
Open direct sourcePublished research
Published physiology of KISS1R signalling and LH release, including desensitization.
Open direct source