GHRP-2
An older, stronger GH-releasing peptide. More effective per dose than Ipamorelin, but with a rougher side-effect profile.
What is GHRP-2?
GHRP-2, also called pralmorelin, is a synthetic hexapeptide that tells your pituitary to release its own growth hormone. It belongs to the same ghrelin-mimetic GHRP family as ipamorelin, but it is older and hits harder. Per dose it drives more GH output than ipamorelin. The tradeoff is a rougher profile: it raises appetite, and at higher doses it nudges cortisol and prolactin up too. In Japan it is approved as pralmorelin, but only as a diagnostic agent for testing growth hormone deficiency, not as a therapy.
How GHRP-2 works
GHRP-2 is an agonist of the ghrelin receptor (GHS-R1a) in the pituitary and hypothalamus. Ghrelin is the body's hunger hormone, and the same receptor also triggers GH release, so GHRP-2 does both: a sharp, pulsatile burst of GH plus a real bump in hunger. Because it works through the ghrelin receptor rather than the GHRH receptor, it is often discussed alongside GHRH analogs like CJC-1295, which act on a separate pathway.
What the research shows
GHRP-2 has been studied in humans since the 1990s. Controlled work found that a 1 mcg/kg dose produced GH responses that exceeded the maximal response to GHRH in healthy adults, and the effect is dose-dependent up to roughly 2 mcg/kg before it plateaus. A separate study in healthy men confirmed that GHRP-2, like ghrelin, reliably increases food intake. So the mechanism and the short-term GH and appetite effects are well documented. What is missing is long-term outcome data for the body-composition and anti-aging uses it is sold for.
Dosage and how it is used
There is no approved dose for these uses. Community and clinic protocols commonly reference roughly 100 to 300 mcg subcutaneously, once to a few times per day, often before sleep or around training. These numbers come from practice and early research, not from modern dose-finding trials, so treat them as convention rather than validated medicine.
→ How to reconstitute GHRP-2: calculator, units to draw & storage
Side effects and safety
GHRP-2 is less selective than ipamorelin, so more of its effects spill outside GH. Short-term reports include strong hunger, water retention, tingling, and, at higher doses, elevated cortisol and prolactin. It is not FDA-approved for anti-aging or body-composition use, and there is no long-term human safety data at the doses people actually use.
- Raises appetite noticeably; can raise cortisol and prolactin at higher doses.
- Well characterized for short-term GH release; limited long-term outcome data.
- Not FDA-approved for these uses. Verify current legal status independently.
Frequently asked questions
Is GHRP-2 stronger than ipamorelin?
Per dose, GHRP-2 drives more growth hormone output. The catch is selectivity. Ipamorelin raises GH cleanly, while GHRP-2 also increases appetite and can raise cortisol and prolactin at higher doses.
Does GHRP-2 make you hungry?
Yes. It activates the ghrelin receptor, the same one the hunger hormone uses, and a controlled study in healthy men found it reliably increases food intake.
Is GHRP-2 approved anywhere?
It is approved in Japan as pralmorelin, but only as a diagnostic agent for testing growth hormone deficiency. It is not approved as a therapy and is not FDA-approved in the United States.
What is GHRP-2 stacked with?
It is often discussed alongside a GHRH analog like CJC-1295, because the two raise GH through different receptors. Combining pathways is a common research approach.
References
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Download the appEducational information only. This is not medical advice. Peptide AI is an informational and tracking platform. Everything on this page is for general education. It is not a substitute for professional medical advice and is not a recommendation to use any compound. Many peptides listed here are research compounds the FDA has not approved for human use. Talk to a qualified, licensed healthcare provider before you start, change, or stop any protocol.