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GHRP-2

Growth hormone releasing peptide for GH stimulation and appetite

GHRP-2 molecular structure

🛑 WADA BANNED - Prohibited in competitive sports as growth hormone releasing peptide

Overview

GHRP-2 (Growth Hormone Releasing Peptide-2, Pralmorelin) is a synthetic hexapeptide that stimulates growth hormone secretion through activation of the ghrelin/growth hormone secretagogue receptor (GHS-R1a). Unlike growth hormone releasing hormone (GHRH), GHRP-2 acts through an independent pathway and produces strong, reliable GH pulses. Research demonstrates GHRP-2 increases appetite through ghrelin-like effects, making it useful when appetite stimulation is desired but potentially problematic for weight management applications. The peptide also stimulates mild increases in prolactin and cortisol compared to more selective secretagogues like Ipamorelin. Studies show synergistic effects when combined with GHRH analogs, producing greater GH release than either peptide alone. GHRP-2 has been investigated for diagnostic use in evaluating pituitary GH reserve and therapeutic applications in growth hormone deficiency states. The peptide requires subcutaneous injection multiple times daily due to its short half-life. Research continues into applications for muscle wasting, wound healing, and age-related GH decline.

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

PralmorelinKP-102GPA-748GHRP Kaken 100growth hormone-releasing peptide-2

Status: Research compound - Growth hormone agonist

CAS158861-67-7
PubChem6918297

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

GH secretagogue researchGrowth hormone deficiency diagnosisWasting and cachexiaAnorexia nervosa (investigational)

Available Evidence

Human

A phase 1 study characterized GHRP-2 pharmacokinetics and GH-releasing pharmacodynamics in children. A case report described one year of intranasal GHRP-2 improving body weight and hypoglycemia in a severely emaciated anorexia nervosa patient. Pralmorelin (GHRP-2) is used clinically in Japan (marketed as GHRP Kaken 100) as a growth hormone stimulation test for diagnosing GH deficiency.

Animal

GHRP-2 potently stimulates GH release in animal models via the ghrelin receptor (GHS-R1a), and combinations with GHRH have been studied for amplified GH responses.

In Vitro

Receptor studies show GHRP-2 is a potent agonist at the ghrelin/growth hormone secretagogue receptor (GHS-R1a).

Uncertain

Therapeutic claims for GHRP-2 in anti-aging, bodybuilding, or general GH replacement are not supported by clinical trials; its established human use is as a diagnostic GH stimulation test.

Key Studies & Findings

2 studies
Clinical1998

Phase 1 study in children characterized the pharmacokinetics and GH-releasing pharmacodynamics of GHRP-2 after subcutaneous administration.

Anecdotal2015

One-year intranasal GHRP-2 use improved body weight and hypoglycemia in a severely emaciated anorexia nervosa patient.

Benefits & Effects

11 documented

Growth hormone stimulation

anecdotal

Fat reduction

anecdotal

Improved strength

anecdotal

Muscle growth

anecdotal

Enhanced recovery

anecdotal

Better sleep

anecdotal

GHD Diagnosis: 83% sensitivity, 88% specificity

clinical

Short Stature: Height velocity 3.7→6.1 cm/year intranasal

clinical

Significant IGF-1 elevation (159.5→239.0 ng/mL in clinical study)

clinicalhormonal

Lean body mass improvement

clinicalbody composition

GH deficiency diagnosis utility

clinicaldiagnostic

Side Effects & Safety

10 reported

Increased appetite

mildcommon

Transient cortisol/ACTH elevation

mildcommon

Potential glucose metabolism effects

moderateuncommon

ACTH/Cortisol elevation

mild

Facial flushing

mild

Strong hunger

mildUncommon

Water retention

mildUncommon

Cortisol/prolactin rise

mildUncommon

Rare dizziness

severeRare

Mild-Moderate side effect

Common Reversible

Onset: Hours

Management: Monitor

Dose-dependent

Limitations & Open Questions

Human data are limited to small phase 1/pharmacokinetic studies, case reports, and diagnostic-test use. No large clinical trials support therapeutic use for GH deficiency, wasting, or anti-aging; long-term safety data are lacking, and its short half-life limits practical use.

Pharmacology

Short-acting peptide secretagogue given by subcutaneous or intranasal administration. It activates the ghrelin receptor (GHS-R1a) to stimulate endogenous GH release (it is not GH itself). The phase 1 pediatric study reported rapid absorption and a short plasma half-life consistent with repeated-dosing protocols.

Reported Research Dosing

Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.

100-300 mcg 2-3x/day

Route: SC
Half-life: ~30 minutes

Frequently Asked Questions

Is GHRP-2 approved by the FDA?

No. It is not FDA-approved as a drug; pralmorelin (GHRP-2) has regulatory approval in Japan for use as a diagnostic GH stimulation test.

How does GHRP-2 raise growth hormone?

It is an agonist at the ghrelin receptor (GHS-R1a) on pituitary somatotrophs, stimulating the release of endogenous GH, with effects amplified when combined with GHRH.

Is GHRP-2 the same as ghrelin?

No. Ghrelin is the endogenous peptide ligand of the GHS-R1a receptor; GHRP-2 is a synthetic small peptide that activates the same receptor.

Research Citations

Related Resources

Quick Facts

Formula

C45H55N9O6

Molecular Weight

817.98

Sequence

D-Ala-D-2Nal-Ala-Trp-D-Phe-Lys-NH2

Mechanism

Growth hormone releasing peptide with hunger stimulation

Safety Information

Research compound only. Limited human safety data available.

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