GHRP-2 (Pralmorelin)

GHRP-2 is a synthetic hexapeptide and ghrelin-receptor (GHS-R1a) agonist that triggers pulsatile release of endogenous growth hormone from the pituitary. In Japan it is approved as pralmorelin for diagnostic GH-stimulation testing.

Growth Hormone & Anti-Aging · Not medical advice.

Evidence: Level 2 · diagnostically approved, clinically studied
Type
Single peptide
Category
Growth Hormone & Anti-Aging
Vial code
GHRP2
Vial sizes
5 mg / 10 mg
Brand names
Pralmorelin (GHRP Kaken, Kaken Pharmaceutical, Japan)
Half-life
~15-60 minutes (subcutaneous, very short)

At a glance

Mechanism of action
GHRP-2 acts as a synthetic agonist at the ghrelin receptor (GHS-R1a) in the anterior pituitary and hypothalamus, inducing a pulsatile GH surge via cAMP/PKC signaling while suppressing somatostatin tone; it also mildly elevates ACTH, cortisol and prolactin.
Benefits & use
Acutely increases GH secretion, dose-dependently raises appetite (ghrelin-like) and is used clinically as a diagnostic GH-stimulation test; off-label research interest centers on body composition, sleep quality and recovery.
Study status
Several human RCTs exist (Laferrère 2005/2006 on appetite, Haruta 2015 intranasal in anorexia, Veldhuis 2007 on GH-pulse waveform), the foundational work of Bowers on the GHRP class, plus Phase III diagnostic data that supported PMDA approval of pralmorelin in Japan in 2004.
Dosing note
No dosing instruction - clinical protocols used subcutaneous infusions (e.g. 1 µg/kg/h) and a diagnostic single-dose IV bolus; research/off-label protocols vary widely and should not be self-applied without medical supervision.

Use in the injection calculator

GHRP-2 (Pralmorelin) is a synthetic peptide hormone and ghrelin-receptor agonist from the growth-hormone secretagogue (GHS) class: the hexapeptide (D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2, ~818 Da) binds GHS-R1a and triggers pulsatile release of endogenous growth hormone (GH) from the pituitary - it does not deliver GH itself. In Japan it is approved as pralmorelin for the diagnosis of GH deficiency in adults and children aged 4 and over.

How does GHRP-2 work?

GHRP-2 acts on a different receptor than classical GHRH analogs such as tesamorelin or sermorelin. It activates the ghrelin receptor (GHS-R1a) in the anterior pituitary and hypothalamus. Downstream signaling runs primarily via cAMP, PLC and protein kinase C, producing:

  • a sharp, short GH pulse (peak ~15-60 min),
  • suppression of somatostatin tone,
  • moderate co-stimulation of ACTH, cortisol and prolactin (weaker than GHRP-6, stronger than ipamorelin),
  • increased appetite (ghrelin-like, but milder than GHRP-6).

What does the evidence say?

Compared with GHRP-6, GHRP-2 is the most potent classical GHRP by peak GH output while producing less appetite stimulation. The human evidence includes several small RCTs:

  • Laferrère et al. (2005) showed that a subcutaneous GHRP-2 infusion increased ad-libitum food intake by ~36% in healthy lean men - a clear ghrelin-mimetic effect.
  • Laferrère et al. (2006) confirmed that obese subjects also respond with increased food intake to the ghrelin agonist GHRP-2.
  • Haruta et al. (2015) reported one year of intranasal GHRP-2 in a severely emaciated anorexia-nervosa patient, with improvements in body weight and hypoglycemia symptoms.
  • Veldhuis et al. (2007) dissected how peripheral signals (e.g. estrogen receptor-α) modulate the waveform of GHRP-2-induced GH secretory bursts.

The Japanese diagnostic approval rests on Phase III data showing that a single IV bolus reliably separates GH-sufficient subjects (peak GH ≥ 15 µg/L) from those with severe adult GH deficiency (clearly below this cut-off).

What is GHRP-2 used for?

  • Approved (Japan): diagnostic GH-stimulation test in adults and children ≥ 4 years (pralmorelin, Kaken Pharmaceutical).
  • Clinically investigated: appetite stimulation in cachexia/anorexia, acute GH-pulse studies, combined provocation tests with GHRH/TRH.
  • Off-label research: body composition, sleep architecture, recovery and tissue repair - none of these are FDA-approved indications.

In research protocols GHRP-2 is often combined with a GHRH analog such as CJC-1295 (without DAC) because the two receptor pathways are complementary and produce a stronger, more physiological GH pulse - a principle we also describe in the CJC-1295/Ipamorelin entry.

How safe is GHRP-2?

Published trial data show a generally favorable safety profile, but with the characteristic class effects of GHRPs:

  • Increased appetite - sometimes desired, sometimes not.
  • Moderate rises in cortisol and prolactin, clinically relevant with repeated high dosing.
  • Flushing, water retention, tingling after bolus injection, usually transient.
  • Possible glucose effects (transient insulin resistance, since GH is anti-insulinergic).

Long-term data on repeated use in healthy adults are sparse; diagnostic single doses are considered well tolerated.

Regulatory status

  • Japan (PMDA, 10/2004): approved as pralmorelin for GH-deficiency diagnosis in adults and children ≥ 4 years.
  • US / EU: no FDA or EMA approval; North American rights were once sublicensed to Wyeth but never progressed.
  • Sport: GHRP-2 is on the WADA Prohibited List at all times (class S2: peptide hormones and growth factors).

How does GHRP-2 compare to GHRP-6 and ipamorelin?

  • GHRP-2 vs GHRP-6: higher GH peak, less hunger, somewhat lower cortisol/prolactin rise.
  • GHRP-2 vs ipamorelin: ipamorelin is far more selective (almost no cortisol/prolactin effect); GHRP-2 delivers a stronger raw GH pulse.
  • GHRP-2 vs GHRH analogs such as tesamorelin: completely different receptor pathway (GHS-R1a vs GHRH-R), so the two are additive when combined.

Frequently asked questions about GHRP-2

Is GHRP-2 legal to buy?

Outside Japan there is no approved pharmaceutical form of GHRP-2. Depending on the country and formulation, it falls under different rules for peptide hormones; self-use without a medical indication and supervision is not recommended.

How long does a dose of GHRP-2 last?

Plasma half-life is very short (~15-60 min) and the GH pulse lasts roughly 1-2 hours. Research protocols therefore use multiple daily doses or combine GHRP-2 with a long-acting GHRH analog such as CJC-1295 with DAC for sustained GH-axis stimulation.

Is GHRP-2 the same as pralmorelin?

Yes. Pramlomrelin is the INN (International Nonproprietary Name) of GHRP-2 as a drug substance. In Japan it is marketed as GHRP Kaken by Kaken Pharmaceutical.

Disclaimer: Peptipedia provides general information on peptides - not medical advice and no dosing or sourcing recommendations. Talk to a clinician you trust before using any peptide.

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