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GHRP-2

GH secretagogue (ghrelin receptor agonist)

Also known as: Pralmorelin, KP-102, GPA-748

Tier 3, Preclinical only

Evidence is limited to animal or in-vitro work. No human pharmacokinetics. Any human dose in circulation is extrapolated, and extrapolation across species routinely fails.

Half-life
Not established

No published human plasma half-life was located, including in the KP-102 pharmacology papers. Urinary excretion data exist for anti-doping purposes, GHRP-2 and its free-acid metabolite are detectable in urine up to 47 hours after administration, but a urinary detection window is NOT a half-life and must not be read as one. A rat study reports ~50% intranasal bioavailability and no half-life.

Dosing
100 mcg

The only sourced human dose is DIAGNOSTIC, not therapeutic: 100 mcg intravenously as a single bolus for the GH-releasing peptide-2 test for adult GH deficiency, with GH measured over the following 2 hours. This is a one-time diagnostic challenge, not a repeated-administration therapeutic dose. No published subcutaneous therapeutic range exists.

Frequency
Single dose in the diagnostic setting only
Regulatory status
Approved in Japan as pralmorelin for diagnostic use in growth hormone deficiency. Not approved in the US for any indication. Prohibited at all times under WADA Prohibited List section S2.
Evidence base
mixed · confidence: low

Approval is narrow and diagnostic, a single-dose challenge test in one country. That is not evidence supporting repeated therapeutic use, which has not been studied.

Safety

GHRP-2 is a ghrelin receptor agonist and co-stimulates ACTH/cortisol and prolactin in addition to GH, a key difference from ipamorelin. Animal general-pharmacology work showed no obvious effect on CNS, autonomic, respiratory, cardiovascular, digestive, renal, or haematologic systems at pharmacological doses. Human safety beyond single diagnostic doses is not characterised; repeated therapeutic use has not been studied.