1. STACK
  2. Compounds
  3. Kisspeptin-10
Hormone signalling

Kisspeptin-10

Also written: KP-10 · metastin (45-54)

Kisspeptin-10: the GnRH-stimulating peptide, its 4-minute human half-life, what Imperial College trials found, FDA Category 2 status, and side effects.

Class
kisspeptin receptor (KISS1R) agonist; hypothalamic GnRH secretagogue
Unit in STACK
Varies by preparation — use what your prescriber gave you
Route
subcutaneous or intravenous (studies); nominated for subcutaneous and intramuscular compounding
Reference half-life
3.8 min
Not FDA-approved

Not an FDA-approved drug; in 503A Category 2 (significant safety risks) since Sep 29 2023, and on Oct 29 2024 the FDA Pharmacy Compounding Advisory Committee voted 0–11 against adding it to the 503A bulks list (no final rule found as of Sep 24 2026).

Last verified against its sources on September 24, 2026. Education and self-tracking only — nothing on this page is medical or dosing advice.

What it is

Kisspeptins are a family of naturally occurring peptides, kisspeptin-10, -13, -14 and -54, named for their number of amino acids; all share the same C-terminal ten-amino-acid sequence, kisspeptin-10, which is required for biological activity [2]. In humans, inactivating mutations of the kisspeptin receptor cause pubertal failure and activating mutations can cause precocious puberty [2]. Kisspeptin-54 is the major circulating form in humans [11]. Kisspeptin-10 is the shortest active fragment; it is simpler to synthesize, which is why it is the form nominated for compounding [2][3]. Most human research comes from Waljit Dhillo’s group at Imperial College London, which has given kisspeptin-10 and kisspeptin-54 intravenously and subcutaneously to healthy volunteers and patients since 2005 [9][13]. It is not an approved drug; compounded drugs are not FDA-approved [14].

How it works

Kisspeptin-10 acts upstream of the pituitary: it stimulates release of GnRH from the hypothalamus, which in turn releases LH and FSH, and the effect disappears if a GnRH antagonist is given first [2]. In healthy men an intravenous bolus raised LH and FSH at doses as low as 0.3 and 1.0 nmol/kg, and a 3 h infusion produced LH and FSH responses similar to kisspeptin-54 but roughly one-third of those from GnRH itself [1][10]. Women respond differently: in the follicular phase, neither intravenous bolus, subcutaneous bolus nor intravenous infusion changed gonadotropins, while in the preovulatory phase an intravenous bolus raised LH and FSH [1]. The longer isoform, kisspeptin-54, is more potent, which the authors attribute partly to the rapid breakdown of kisspeptin-10 in the circulation [2].

What the evidence shows

Human studies are small physiological experiments, typically four to five volunteers per dosing group [1][10]. A 2026 Imperial study in 15 healthy men found that 8 h daily subcutaneous infusions of kisspeptin-10 for 12 days sustained higher LH and FSH, while continuous infusion for 5 days left gonadotropins no different from vehicle even though testosterone stayed elevated [13]. The clinical trials that reached patients used kisspeptin-54, not kisspeptin-10: a single subcutaneous injection triggered egg maturation in 53 women undergoing IVF, with a 23% clinical pregnancy rate [11], and in 60 women at high risk of ovarian hyperstimulation syndrome, maturation occurred in 95% and no woman developed moderate or severe OHSS [12]. FDA’s 2024 review found no published trials assessing safety of kisspeptin-10 given for more than a day, no intramuscular studies, and noted that approved products already exist for secondary hypogonadism [3].

Regulatory status

Kisspeptin-10 is not an FDA-approved drug [14]. It was nominated for the 503A bulks list for treatment of secondary hypogonadism in men [3][5]. On Sep 29 2023 FDA placed it in 503A Category 2, citing possible immunogenicity by injection, peptide-related impurities and no or only limited safety information for the proposed routes [6]. For Category 2 substances FDA says it “would consider taking action against a compounder” under its general enforcement policies [8]. It remains in Category 2 on the list updated May 14 2026 [7]. At the Oct 29 2024 advisory committee meeting FDA proposed that kisspeptin-10 not be included; the vote was Yes 0, No 11, Abstain 0, and the committee “unanimously agreed” it should not be listed given the lack of convincing safety and efficacy data [4]. As of Sep 24 2026 we found no final rule.

Half-life and what it means for a level curve

The reference half-life in STACK is 0.063 hours, which is 3.8 minutes. Jayasena et al. sampled blood every one to two minutes after stopping an intravenous infusion of 360 pmol/kg/min and calculated plasma half-lives of 3.8 ± 0.3 min in men and 4.1 ± 0.4 min in women in both the follicular and preovulatory phases, with no significant difference between groups [2]. FDA’s briefing cites the same 3.8 min figure [3]. That is about seven-fold shorter than kisspeptin-54, whose plasma half-life was 27.6 ± 1.1 min in men [2][9]. No subcutaneous half-life has been published, and FDA notes that subcutaneous concentration-time profiles differ from intravenous ones [3]. With a 4 min half-life, a level reaches about 97% of steady state after roughly five half-lives, around 20 minutes, and falls back to near zero just as fast; the hormone response outlasts the peptide. STACK’s curve is an estimate from this published half-life, not a blood level.

Reported side effects

The Imperial studies recorded heart rate, blood pressure and adverse symptoms at regular intervals [2]. FDA’s summary of the published studies found no serious adverse events, but stressed that the studies were short, small and often did not report adverse events at all [3]. FDA’s adverse event database contained one report through Oct 25 2023: a 17-year-old male with hypogonadotropic hypogonadism given a compounded kisspeptin-10 product subcutaneously daily for six weeks gained weight and had a rise in estrone, which were not the intended effects; the report lacked medical history and concomitant medications [3]. FDA’s stated concerns are immunogenicity, which is higher for subcutaneous than intravenous peptides, and aggregation or impurities in an under-characterized bulk substance [3]. Call your prescriber about any reaction, including unexpected weight change or breast tenderness.

Storage and handling

FDA’s chemistry review quotes the nominator’s certificate of analysis: lyophilized kisspeptin-10 should be stored at 2–8°C for less than six months and at −20°C for longer, kept sealed with desiccant and protected from light because the peptide is hygroscopic and light-sensitive; the reconstituted preparation is reported to be stable when stored at 2–8°C [3]. There is no approved label, so the compounding pharmacy’s label governs your refrigeration instructions and beyond-use date. FDA does not verify the safety, effectiveness or quality of compounded drugs before they are marketed [14]. If your product is a powder, STACK’s reconstitution calculator does the concentration math; it never suggests what to take.

What STACK tracks for it

STACK logs each kisspeptin-10 dose as your prescriber wrote it, in mcg, with the route, time of day and injection site. The estimated-level curve uses the 3.8 min intravenous half-life, so it will show a brief spike and a return to baseline within about 20 minutes; that is a property of the peptide, not a sign a dose was missed. If your prescriber orders hormone labs, you can record LH, FSH, testosterone or estradiol results on the same timeline to see them against dosing days. Side-effect entries, weight, and vial inventory with the pharmacy lot number and beyond-use date are kept alongside any other compounds in your plan.

The reference half-life in STACK

STACK's simulator and the app use 3.8 min for Kisspeptin-10: ~4 min (3.8 ± 0.3 min in men; 4.1 ± 0.4 min in women), intravenous. Measured in: healthy men and healthy women (follicular and preovulatory phases), after intravenous infusion.

Kisspeptin-10

3.8 min · measured intravenous

Reference half-life of about 4 minutes (0.063 h) is the intravenous value; no subcutaneous half-life is published. Editable. Educational only — not medical or dosing advice.

“Plasma half-life of 3.8 ± 0.3 min in men and 4.1 ± 0.4 min in women after intravenous infusion.” — Jayasena CN, Nijher GM, Comninos AN, et al. The effects of kisspeptin-10 on reproductive hormone release show sexual dimorphism in humans (2011). Journal of Clinical Endocrinology & Metabolism · PMC3232613. View source

Estimate only. Modelled from the published half-life you selected and the doses you logged — not a measured blood level. Do not use it to make medication decisions.

Free tools for Kisspeptin-10

Read next

Sources

Every URL below was fetched and checked on 2026-09-24. Bracketed numbers in the text link here.

  1. TrialThe effects of kisspeptin-10 on reproductive hormone release show sexual dimorphism in humans (Jayasena et al. 2011, PubMed record)
  2. TrialThe Effects of Kisspeptin-10 on Reproductive Hormone Release Show Sexual Dimorphism in Humans (Jayasena et al. 2011, full text)
  3. FDAFDA Briefing Document, PCAC Meeting Oct 29 2024: Kisspeptin-10
  4. FDAOctober 29, 2024 Meeting of the Pharmacy Compounding Advisory Committee: Minutes
  5. FDAOctober 29, 2024: Meeting of the Pharmacy Compounding Advisory Committee
  6. FDACertain Bulk Drug Substances for Use in Compounding that May Present Significant Safety Risks
  7. FDABulk Drug Substances Nominated for Use in Compounding Under Section 503A (updated May 14, 2026)
  8. FDABulk Drug Substances Used in Compounding Under Section 503A of the FD&C Act
  9. TrialKisspeptin-54 stimulates the hypothalamic-pituitary gonadal axis in human males (Dhillo et al. 2005)
  10. TrialDirect comparison of the effects of intravenous kisspeptin-10, kisspeptin-54 and GnRH on gonadotrophin secretion in healthy men (Jayasena et al. 2015)
  11. TrialKisspeptin-54 triggers egg maturation in women undergoing in vitro fertilization (Jayasena et al. 2014)
  12. TrialEfficacy of Kisspeptin-54 to Trigger Oocyte Maturation in Women at High Risk of OHSS During IVF Therapy (Abbara et al. 2015)
  13. TrialChronic subcutaneous kisspeptin-10 stimulates gonadotropin secretion for 12 days in healthy men (Yeung et al. 2026)
  14. FDACompounding and the FDA: Questions and Answers