Library / GH axis / Ipamorelin

Ghrelin-receptor agonist · GHRP analog

Ipamorelin

Cited range No current US approval

ClassSelective GHSR-1a agonist
Half-life~2 hours (commonly cited)
Routes in sourcesSC pulses
Often paired withCJC-1295 no-DAC / tesamorelin / sermorelin

What it is

Ipamorelin (NNC 26-0161) is a pentapeptide growth-hormone secretagogue designed to be more selective than older GHRPs. It was explored clinically, then development stopped; it is not an approved GH therapy.

Benefits in plain language

What researchers and reference users usually mean when they talk about this compound. These are study themes and common claims — not a promise that it will do this in you.

If a branded, FDA-approved product exists, that label is the only dose that is actually authorized. Research-chemical vials are a different object.

Mechanism of action

It stimulates the ghrelin receptor on pituitary somatotrophs, prompting a GH pulse. Relative to hexarelin or GHRP-6 it is described as having less ACTH/cortisol and prolactin spillover in early studies — still not “side-effect free.”

Possible side effects / caveats

Reported or expected: water retention, joint stiffness, tingling, increased appetite in some users of this class, and theoretical effects of repeated GH/IGF-1 elevation. Compounding and research vials vary widely in content.

Protocol ranges

Source tierAmountFrequencyNotes
Cited range100–300 mcg per pulse1–3× dailyMost repeated secondary figure
Cited stack pattern100–200 mcg + a GHRH analogSame sittingGHRH + GHRP synergy is pharmacological folklore plus some experimental basis