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All peptides
GHRP / ghrelin mimetic

Ipamorelin

Also known as: NNC 26-0161

Tier 3 — Animal / in vitroReviewed 2026-04-30

Selective GH secretagogue with minimal cortisol or prolactin elevation in animal studies. Human evidence is limited.

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Overview

Ipamorelin is a synthetic pentapeptide that acts at the ghrelin receptor (GHS-R1a) to stimulate pituitary growth hormone release. It was developed in the 1990s as a more selective GHRP than GHRP-2 or GHRP-6, with much less cortisol and prolactin elevation in early animal and short human studies. It was investigated for postoperative ileus before development was discontinued, so the published human dose-finding evidence is shallower than its popularity in self-experimenter communities suggests.

Mechanism

Selective agonism of the GHS-R1a (ghrelin receptor) on pituitary somatotrophs and the arcuate nucleus, triggering pulsatile endogenous GH release. Selectivity for GH over ACTH, prolactin, and FSH/LH distinguishes it from older GHRPs.

Evidence by indication

We classify each indication separately. The same peptide can be Tier 1 for one use and Tier 4 for another. Tiers reflect the published literature, not the strength of community framing.

Stimulation of GH release in healthy adults

Tier 2medium confidence

Small human studies (Raun et al. and follow-ups) demonstrated selective GH release with minimal effect on cortisol or prolactin. These are short-duration pharmacology studies, not outcome trials.

Postoperative ileus

Tier 2medium confidence

A Phase 2b RCT in postoperative ileus showed mixed results and development was halted. Worth knowing: the only large-scale human RCT for ipamorelin is in this discontinued indication, not the body-composition claims it is sold against today.

Body composition / muscle gain

Tier 3high confidence

No published human RCTs evaluate ipamorelin (alone or stacked) for hypertrophy, body fat reduction, or athletic performance. Claims rest on extrapolation from GH/IGF-1 elevation rather than direct measurement of body-composition outcomes.

No primary citations are anchored to this indication — the tier reflects the absence of usable literature, not a missing reference.

Sleep quality

Tier 3medium confidence

GH pulses occur predominantly during slow-wave sleep, and GHRP/GHRH pairings can amplify these. There are no controlled human trials specifically of ipamorelin and sleep architecture, however.

No primary citations are anchored to this indication — the tier reflects the absence of usable literature, not a missing reference.

Studied dose ranges

The ranges below come from published trial protocols where available, and from documented self-experimenter consensus where the literature does not include human dose-finding work. The notes flag which is which.

100300 mcg1–3× daily · subcutaneous

Most published human dose ranges fall between 100–300 mcg per injection, often paired with a GHRH analog (e.g., CJC-1295 or sermorelin). Higher doses do not produce proportionally larger GH pulses.

Contraindications

  • Active malignancy (relative — GH/IGF-1 is theoretically permissive of tumor growth)
  • Pregnancy and breastfeeding
  • Severe insulin resistance or uncontrolled diabetes (GH is counter-regulatory to insulin)
  • Pituitary or hypothalamic disease — confirm with provider before use
  • Hypersensitivity to ipamorelin

Reported side effects

  • Injection site reactions
  • Transient hunger increase (ghrelin-receptor effect)
  • Headache
  • Fluid retention with chronic use
  • Mild fatigue or drowsiness shortly after dosing
  • Possible insulin sensitivity decrease at higher cumulative doses

Reconstitution & storage

Most ipamorelin sold for research is a lyophilized powder reconstituted with bacteriostatic water (BAC). Aim for a concentration that yields ergonomic doses on a U-100 syringe — 5 mg in 2 mL gives 2.5 mg/mL, putting a 200 mcg dose at 8 units. Use the calculator to verify.

Storage. Lyophilized vial: room temperature is acceptable short-term; refrigeration (2–8 °C) extends stability. Reconstituted: refrigerate 2–8 °C, use within 30 days. Avoid repeated temperature cycling.

Open the peptide calculator → to compute exact draw volumes for your specific vial and BAC water choice.

Editorial note

Ipamorelin's reputation outpaces its evidence. The selective-GH-release pharmacology is real and replicated; the clinical-outcome story is not. Resist tier inflation.

Citations

  1. [1]
    Ipamorelin, the first selective growth hormone secretagogue
    Raun K, Hansen BS, Johansen NL, et al. · European Journal of Endocrinology · 1998 · PMID 9789012
    Original characterization of ipamorelin's GH selectivity.
    View source
  2. [2]
    Effect of ipamorelin, a novel selective growth hormone secretagogue, on the recovery of GI function in postoperative ileus
    Beck DE, Sweeney WB, McCarter MD, et al. · International Journal of Colorectal Disease · 2014 · PMID 24309627
    Phase 2b RCT in postoperative ileus — the largest human dataset for ipamorelin.
    View source