Research onlyGrowth hormoneIntravenousEvidence 3/5

GHRP-2

Also known as: Pralmorelin, KP-102

GHRP-2 is a synthetic hexapeptide ghrelin mimetic that activates the growth hormone secretagogue receptor (GHS-R1a) at the hypothalamus and pituitary, amplifying GHRH and reducing somatostatin tone to drive a transient growth hormone pulse.

GHRP-2
Drug class
Growth hormone secretagogue / ghrelin receptor (GHS-R1a) agonist (synthetic hexapeptide)
Primary targets
Growth hormone secretagogue receptor (GHS-R1a), Ghrelin receptor, Anterior pituitary somatotrophs, Hypothalamic GHRH/somatostatin neurons
Dose reference
Diagnostic use only (not a therapeutic recommendation): single 100 microgram IV bolus in adults, or ~2 micrograms/kg IV in children, for GH-deficiency provocative testing
Half-life
Short; GH response peaks ~15-60 min after IV dosing and clears within a few hours (precise human half-life not consistently reported)
Developer / origin
Kaken Pharmaceutical (Japan); compound originated from the GHRP work of Bowers and colleagues
Reference year
2004
Evidence score
3/5 - Validated GH-deficiency diagnostic; no established therapeutic use
Evidence 3/5

Validated GH-deficiency diagnostic; no established therapeutic use

GHRP-2 has solid primary-source human evidence as a single-bolus growth hormone secretagogue used to diagnose GH deficiency, including a regulatory approval in Japan. Evidence for any chronic therapeutic, body-composition or anti-aging use is absent, and off-target ACTH, cortisol, prolactin and appetite effects are documented.

Limited human pharmacology or small clinical evidence.

Evidence basis

  • Approved in Japan as a single-dose pralmorelin diagnostic for GH deficiency; validated GH cut-offs in adults (~15 ug/L) and children
  • Randomized human studies show GHRP-2 raises food intake like ghrelin in lean and obese subjects
  • Documented direct ACTH-releasing activity and cortisol/prolactin elevation in human pituitary testing
  • No FDA approval and no validated therapeutic indication; development for GHD/short-stature treatment did not reach market
  • Long-term, repeated-dose human safety data are lacking because approved use is a one-time provocative test

How to read this entry

Dose references and half-life values are pulled from trial protocols, labels, reviews, or published summaries where available. They are context for research and comparison, not a personal dosing recommendation.

Status matters: approved drugs have regulated indications; investigational compounds are still being studied; research-only peptides do not have established human dosing, safety, or efficacy for consumer use.

GHRP-2 guides

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Selectively stimulates pituitary growth hormone release without significant cortisol or prolactin elevation seen with older GHRPs.

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A modified IGF-1 that binds IGF binding proteins far more weakly than native IGF-1, leaving it free to act as a potent, long-acting agonist at the IGF-1 receptor.

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