PeptaHub
The comprehensive peptide reference
MUSCLE & GROWTHPEPTIDE PROFILE

Hexarelin

Also known as Examorelin, HEX

Hexarelin is one of the most potent synthetic growth hormone releasing peptides (GHRPs), producing the strongest GH release of any GHRP. It is a hexapeptide analog of GHRP-6 with a methylated tryptophan residue that increases its potency. Beyond GH release, hexarelin has notable cardioprotective properties, acting directly on cardiac tissue independent of GH. It was studied in clinical trials for heart failure.

Last updated April 10, 2026

TL;DR

Quick summary

Hexarelin is the most potent GHRP, producing up to 7x baseline GH spikes via the ghrelin receptor. Beyond GH release, it has notable cardioprotective properties acting directly on cardiac tissue, and was studied in Phase II heart failure trials.

§ 01

Overview

Hexarelin is one of the most potent synthetic growth hormone releasing peptides (GHRPs), producing the strongest GH release of any GHRP. It is a hexapeptide analog of GHRP-6 with a methylated tryptophan residue that increases its potency. Beyond GH release, hexarelin has notable cardioprotective properties, acting directly on cardiac tissue independent of GH. It was studied in clinical trials for heart failure.

§ 02

Mechanism of action

Hexarelin binds to the ghrelin receptor (GHS-R1a) in the pituitary and hypothalamus, stimulating robust GH release. It produces the highest GH spike of any GHRP (up to 7x baseline). It also activates cardiac GHS receptors (GHS-R1a in cardiomyocytes), providing direct cardioprotection: reducing cardiac fibrosis, improving ventricular function, and protecting against ischemia-reperfusion injury. Unlike Ipamorelin, hexarelin does increase cortisol and prolactin at higher doses.

§ 03

Dosing protocols

PurposeRouteDosageFrequency
GH release / body compositionsubcutaneous100200 mcg2-3x daily

Dosing information is for educational purposes only. Consult a qualified healthcare professional before using any peptide.

§ 04

Research summary

Clinical studies confirm potent GH release (5-7x baseline) with dose-dependent response. Phase II heart failure trials showed improved cardiac function (increased LVEF, reduced wall stress) independent of GH effects. Cardioprotective effects demonstrated in post-MI patients and animal models. GH response attenuates with chronic use (desensitization of GHS-R1a), recommending cyclic use. Side effects include increased cortisol and prolactin at doses above 2mcg/kg, appetite stimulation, and water retention.[1][2][3][4][5]

📄This section cites 5 peer-reviewed sources. View all references →
§ 04b

Evidence grading

Each claimed benefit is graded by the strength of available evidence. Grades reflect study quality, not effect size.

moderate
Growth hormone stimulationLaron et al. Clin Endocrinol 1995: human dose-ranging study in GH-deficient and normal adults confirming potent GH pulse; among the most potent GHRPs tested in humans
preliminary
Cardiac protection after ischemia-reperfusion injuryRossoni et al. J Cardiovasc Pharmacol 1999: isolated rat heart model; hexarelin reduced infarct size via CD36 receptor; no human cardiovascular trials
moderate
Tachyphylaxis (desensitization) with repeated dosingMultiple human studies showing blunted GH response with continued daily dosing; significant loss of efficacy within 4–8 weeks — a well-documented limitation
moderate
Growth hormone deficiency diagnosisUsed as a diagnostic provocation test in European endocrinology; Phase 2 data in GHD adults showing reliable somatotroph stimulation
insufficient
Muscle mass and recovery in agingAnecdotal use only; no published clinical trials with muscle mass or functional outcomes as primary endpoints

Strong = multiple RCTs · Moderate = limited trials or observational · Preliminary = animal or in vitro only · Insufficient = anecdotal or no published data

§ 05

Side effects

Increased cortisol (dose-dependent)
Increased prolactin
Water retention
Appetite stimulation
Flushing
Injection site pain

Side effects vary by individual. This is not an exhaustive list. Report unusual symptoms to a healthcare professional.

§ 06

Common stacks

Peptides commonly paired with Hexarelin for synergistic effects.

§ 08

Sourcing & access

Research compound

Hexarelin is classified as a research compound. Regulatory status varies by jurisdiction. Always verify current legal status and source from vendors providing third-party certificates of analysis (COA).

§ 09

Frequently asked questions

Hexarelin (Examorelin) is a synthetic hexapeptide growth hormone releasing peptide and one of the most potent GHRPs available. It produces the strongest GH release of any GHRP and has unique cardioprotective effects independent of growth hormone.

Hexarelin produces higher GH spikes (up to 7x baseline vs 3-5x for Ipamorelin) but also increases cortisol and prolactin at higher doses. Ipamorelin is considered cleaner with fewer side effects, while Hexarelin is chosen for maximum GH output and cardiac benefits.

Yes, Phase II heart failure trials showed Hexarelin improved cardiac function by increasing left ventricular ejection fraction and reducing wall stress. These cardioprotective effects are mediated through direct activation of GHS receptors on cardiomyocytes, independent of GH.

Yes, GH response attenuates with continuous use due to desensitization of the GHS-R1a receptor. Cyclic use of 4 to 8 weeks on, followed by 4 weeks off, is recommended to maintain effectiveness.

Common protocols use 100 to 200 mcg injected subcutaneously 2 to 3 times daily on an empty stomach. Keeping doses moderate helps limit the dose-dependent cortisol and prolactin elevation seen above 2 mcg per kg. Cycling 4 to 8 weeks on followed by 4 weeks off helps avoid GHS-R1a desensitization.

§ 10

Research references

  1. The cardiovascular action of hexarelinBroglio F, Prodam F, Me E, et al.Journal of Endocrinological Investigation, 2014PubMed
  2. Effects of acute hexarelin administration on cardiac performance in patients with coronary artery disease during by-pass surgeryBisi G, Podio V, Valetto MR, et al.European Journal of Pharmacology, 2002PubMed
  3. The Growth Hormone Secretagogue Hexarelin Protects Rat Cardiomyocytes From in vivo Ischemia/Reperfusion Injury Through Interleukin-1 Signaling PathwayMa Y, Zhang L, Launikonis BS, Chen C.Frontiers in Physiology, 2017PubMed
  4. Mechanism of action of Hexarelin. I. Growth hormone-releasing activity in the ratGhigo E, Arvat E, Muccioli G, Camanni F.European Journal of Endocrinology, 1996PubMed
  5. The Safety and Efficacy of Growth Hormone SecretagoguesSigalos JT, Pastuszak AW.Sexual Medicine Reviews, 2018PubMed
● READER REVIEWS

What readers say about Hexarelin

No reader reviews yet. If you’ve used Hexarelin, share your experience — your review helps the next person decide.