Peptika.
Cat. 03
Type I · Lyophilised
PK-2026-GHRP-6
Peptika GHRP-6 vial
Lot-tracedEU pharmacyCold-chain 2–8 °C
03 · Growth Hormone

GHRP-6.

First-generation GH-releasing hexapeptide with appetite-stimulating side effect.

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 GHRP-6.

GHRP-6 is a hexapeptide and one of the earliest synthetic ghrelin-receptor agonists developed. It produces a strong GH pulse and is also known for a characteristic appetite-stimulating side effect, which can be useful in cachectic or low-appetite patients but undesirable in body-composition protocols.

Compared with Ipamorelin, GHRP-6 is less selective for GHS-R1a, so it can produce modest cortisol and prolactin elevations. Modern protocols generally favour ipamorelin unless the appetite effect is specifically wanted.

Mechanism of action

GHRP-6 activates the ghrelin / GHS-R1a receptor on pituitary somatotrophs, releasing GH in a pulsatile fashion. It also signals through ghrelin receptors in the hypothalamic arcuate nucleus, which drives the appetite effect.

Posology · for information only

Subcutaneous injection, typically 100 mcg, 2–3 times per day. Bedtime administration leverages the natural nocturnal GH peak.

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
GH pulse amplificationAppetite supportCachectic states (research)
Identification & specifications
INN / Name
GHRP-6
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.