Growth Hormone Secretagogue
GHRP-2
Also known as: Pralmorelin
A synthetic hexapeptide growth hormone secretagogue with a genuine pediatric human clinical trial history, distinguished from more selective secretagogues like ipamorelin by also stimulating ACTH/cortisol release and appetite.
Overview
GHRP-2 (pralmorelin) is a synthetic hexapeptide growth hormone secretagogue that acts through the same ghrelin receptor (GHS-R1a) pathway as GHRP-6 and hexarelin. Unlike more recently developed, more selective secretagogues such as ipamorelin, GHRP-2 also stimulates ACTH/cortisol release and appetite as documented side effects of its GH-releasing activity.
Proposed Mechanism of Action
GHRP-2 activates GHS-R1a at both pituitary and hypothalamic sites, stimulating GH release through calcium-channel and protein kinase C-linked signaling — the same receptor ghrelin (the body's endogenous "hunger hormone") acts on, which is the likely basis for GHRP-2's reported appetite-stimulating side effect.
Research Context
The cited study is a genuine pediatric human clinical trial: children with short stature received intranasal GHRP-2 and showed both an acute GH response and, over 6-24 months, meaningfully increased height velocity compared to their own pre-treatment baseline. This is more direct human outcome data than exists for several other GH secretagogues covered on this site.
Limitations of the Current Evidence
- The cited trial is in children with diagnosed short stature — a specific clinical population, and results (height velocity increases) reflect a growth-plate-open pediatric context that doesn't extend to adult use claims.
- GHRP-2's non-selective hormonal profile (raising ACTH/cortisol alongside GH) is a meaningful practical difference from newer secretagogues like ipamorelin — the two are not interchangeable despite both being called "GH secretagogues."
Research-Setting Dosing (as reported in literature)
| Route | Range (as reported) | Frequency | Notes |
|---|---|---|---|
| Intranasal | 5–20 µg/kg | — | Pihoker et al. (1997); each child showed a GH response >10 µg/L to intranasal GHRP-2 in this dose range. Height velocity increased from 3.7 ± 0.2 cm/year at baseline to 6.1 ± 0.3 cm/year at 6 months in treated children. |
Figures above are extracted directly from the cited preclinical/research literature. They describe what researchers administered to study subjects (frequently animal models) — they are not human dosing recommendations and are not medical advice.
Cited Studies
Treatment effects of intranasal growth hormone releasing peptide-2 in children with short stature
Pihoker C, Badger TM, Reynolds GA, Bowers CY · Journal of Endocrinology · 1997
Human clinical trial (children with short stature)View source →
Last updated August 1, 2026