Peptika.
Cat. 05
Type I · Lyophilised
PK-2026-KISSPE
Peptika Kisspeptin-10 vial
Lot-tracedEU pharmacyCold-chain 2–8 °C
05 · Reproductive & Hormonal Health

Kisspeptin-10.

Kiss1-derived decapeptide — upstream regulator of GnRH and the reproductive axis.

Select strengthPer-vial price
Quantity
1
Total
€50.00· 1 vial

Build your bag, then either book a consultation (an EU-licensed physician reviews your file — anything declined is refunded) or upload an existing Rx at checkout.

  • Magistral preparation — Directive 2001/83/EC Art. 5(1).
  • Patient-named prescription only — dispensed against a valid Rx.
  • EU-GMP Annex 1 Grade A/B cleanroom compounding.
  • Cold-chain shipping across EU/EEA — 2–5 working days.
Overview

About Kisspeptin-10.

Kisspeptin-10 is the active C-terminal decapeptide of kisspeptin, the master regulator of the hypothalamic-pituitary-gonadal axis. Loss-of-function mutations in the Kiss1 receptor (KISS1R) cause idiopathic hypogonadotropic hypogonadism.

Clinical research has examined kisspeptin in fertility and sexual-arousal contexts, with a particularly interesting profile for women with hypothalamic amenorrhea.

Mechanism of action

Kisspeptin binds KISS1R on hypothalamic GnRH neurons, triggering pulsatile GnRH release. This drives LH and FSH secretion from the pituitary and downstream sex-hormone production.

Posology · for information only

Subcutaneous or intravenous injection, typically 50–100 mcg per dose; protocols vary widely by indication.

Your physician sets the prescription. This is descriptive information, not a self-administration guide.

Storage

Lyophilised: store at 2–8 °C, protect from light. Once reconstituted: 2–8 °C, use within 30 days. Do not freeze.

Evidence baseClinical RCT evidence
Indications studied
HPG-axis supportSexual arousal (research)Fertility adjunct
Identification & specifications
INN / Name
Kisspeptin-10
Form
Lyophilised vial · subcutaneous injection
Strength
5mg vial
Manufacturing
EU-GMP Annex 1 · Grade A/B
Endotoxins
European Pharmacopoeia 2.6.14 · LAL assay
Identity & purity
HPLC + MS · > 98%
Cold chain
Validated 2–8 °C, monitored end-to-end
Regulatory basis
Directive 2001/83/EC · Article 5(1)
Logistics

2–5 working days

EU / EEA cold-chain delivery, 2–8 °C monitored end-to-end with digital temperature log. Tracking link sent on dispatch.

Legal status

Magistral preparation

Patient-named preparation under Directive 2001/83/EC Article 5(1). Dispensed exclusively against a valid EU prescription.

Cross-border

EU prescription recognition

Prescriptions written in one EU member state are recognised in others under Directive 2011/24/EU on cross-border healthcare.