Ipamorelin vs GHRP-2

Both hit the same receptor, and selectivity is the whole difference

Both are ghrelin receptor agonists that trigger growth hormone release, so on paper they do the same job. Ipamorelin is the selective one: human studies found it raised growth hormone without meaningfully moving cortisol, prolactin or ACTH, and without much appetite effect. GHRP-2 is stronger but less clean, nudging cortisol and prolactin upward and stimulating hunger. GHRP-2 is actually approved in Japan as a diagnostic test; ipamorelin reached phase 2 for post-surgical bowel recovery, missed its endpoint, and was dropped.

Pituitary secretory cell with granular cytoplasm, a large nucleus and tiny secretory vesicles, macro cellular view. Ipamorelin Growth hormone Full entry → Midsagittal human brain cutaway showing the hypothalamic-pituitary region. GHRP-2 Growth hormone Pralmorelin, KP-102 Full entry →
Ipamorelin compared with GHRP-2
Ipamorelin GHRP-2
Evidence behind itHuman trialsHuman trials
Worth knowing

The phase 2 bowel trials did not meet their endpoint and development stopped.

Also nudges cortisol and prolactin up. Appetite stimulation is strong enough to be unwanted for some.

ApprovalIn trialsApproved · Japan
CategoryGrowth hormoneGrowth hormone
What it is

A five-amino-acid peptide that activates the ghrelin receptor to release growth hormone. It is known for selectivity: in studies it raised growth hormone without meaningfully changing cortisol, prolactin or ACTH, and with little effect on appetite.

A six-amino-acid synthetic peptide that activates the ghrelin receptor, prompting the pituitary to release growth hormone. Like ghrelin it also increases appetite, and it can raise cortisol and prolactin somewhat, so it is less selective than ipamorelin.

How it works

Binds the pituitary ghrelin receptor to trigger pulsatile growth hormone release, with notably little effect on cortisol, prolactin or appetite.

Activates the ghrelin receptor on the pituitary, triggering growth hormone release. It also nudges cortisol and prolactin upward, which is what separates it from the more selective ipamorelin.

What studies report
  • Clean growth hormone release without raising cortisol, prolactin or ACTH in human studies
  • Studied for restarting bowel movement after abdominal surgery
  • Reliable growth hormone release in human studies, used diagnostically in Japan
  • Increased appetite and food intake
  • Rise in IGF-1 with repeated use
Dosing

From studies

  • 0.1–2 mg, intravenous, single dose — Human pharmacology studies of growth hormone response. Dose-dependent GH release without raising cortisol or prolactin

Reported, not evidence

  • 200–300 mcg, usually before bed to match the natural GH pulse
  • Commonly 5 days on, 2 off
  • Almost always paired with CJC-1295 without DAC

From studies

  • 100 mcg, intravenous — Diagnostic GH stimulation testing (approved use in Japan). Reliable GH release

Reported, not evidence

  • 100–200 mcg, up to a few times daily
  • Chosen over GHRP-6 when appetite stimulation is unwanted
Why people take itLean muscle preservationFat lossTissue repairRecoveryGrowth hormone release without appetite or cortisol effectsBody compositionGrowth hormone releaseAppetite stimulationRecovery and sleep
In practice
  • Typically taken at night to mimic the body's natural growth hormone pulse
  • Very commonly stacked with CJC-1295 — the pairing is close to a default
  • Preferred over GHRP-2 and GHRP-6 by people who dislike hunger and cortisol effects
  • Sold pre-blended with tesamorelin in a single vial, pairing a secretagogue with a growth hormone releasing factor
  • Chosen over GHRP-6 when appetite stimulation is unwanted
RouteSubcutaneous injection, from reconstituted lyophilised powderSubcutaneous injection, from reconstituted lyophilised powder

Rows describing reported use say what people do, not what has been shown to work. Evidence strength is graded the same way across the whole library, so the two columns are directly comparable.

Read the full entries

Other comparisons

Educational information only. Nothing here is medical advice, a dosing protocol, or a recommendation to use any compound. Comparing two compounds is not a suggestion to take either one. Talk to a licensed clinician before acting on anything you read here. How to read these entries.