Peptide Protocol

GHRP-2: potent GH pulse — cortisol aware.

Second-generation growth hormone-releasing peptide. Strong GH output with some cortisol and prolactin elevation. SubQ 2–3× daily.

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100–300 mcg
Per Dose
8–12 wks on / 4 off
Cycle
SubQ
Route
2–3× daily
Frequency
Overview

What is GHRP-2?

GHRP-2 is a synthetic hexapeptide analog of ghrelin that binds GHS-R1a receptors in the pituitary and hypothalamus, triggering robust GH release. It was one of the first GHRPs extensively studied in human clinical trials. A saturation dose of 100 mcg produces near-maximal GH response; doses above this increase side effects without proportionally increasing GH.

The compound occupies a position between Ipamorelin (cleanest profile) and Hexarelin (most potent) in the GHRP family. It elevates cortisol and prolactin to a modest degree, making it less ideal for long cycles compared to Ipamorelin but more tolerable than older GHRPs. It is commonly combined with a GHRH analog (CJC-1295 No DAC or Sermorelin) for synergistic GH release.

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GHS-R1a Agonism
Binds ghrelin receptors in the pituitary somatotrophs, triggering GH vesicle release via calcium-dependent intracellular signaling cascades.
Hypothalamic Amplification
Also acts at the hypothalamus to suppress somatostatin (GH inhibitor), further amplifying GH output when co-administered with GHRH analogs.
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Dose-Dependent GH Release
GH response scales with dose up to ~100 mcg (saturation point). The GHRH + GHRP-2 combo produces additive effects — 100 mcg GHRH + 30 mcg GHRP-2 is synergistic.
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Cortisol / Prolactin Elevation
Modest ACTH and cortisol elevation occurs at standard doses. Less than GHRP-6 or Hexarelin, but more than Ipamorelin.
Dosing Protocol

Dosing Schedule

Parameters documented in published preclinical and clinical research.

⚠️ Research use only. The following documents parameters from published preclinical and clinical research. Not medical advice. Not for human consumption. Consult a licensed healthcare professional before any use.
PhaseDoseFrequencyDurationNotes
Start50–100 mcgOnce daily (bedtime)Days 1–7Fasted SubQ. 100 mcg is the approximate saturation dose.
Working dose100 mcg2× dailyWeeks 2–8AM fasted + bedtime. Stack with CJC-1295 No DAC 1:1.
Advanced100 mcg3× dailyWeeks 3–12Third dose post-workout. Doses above 100 mcg rarely add GH.
Off cycle4 weeksPrevent receptor desensitization before restarting.
Safety Profile

Safety & Side Effects

✓ Generally Well Tolerated
Extensively studied in human clinical trials
Less appetite stimulation than GHRP-6
Strong GH output at low doses (100 mcg saturation)
Short half-life — dose-timing flexibility
⚠ Potential Concerns
Modest cortisol and prolactin elevation
WADA S2 prohibited
Receptor desensitization with prolonged continuous use
GH blunted by food / elevated blood glucose
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Research use onlyThis page is an educational reference. None of this constitutes medical advice. Consult a qualified professional before any use. All compounds are for research purposes only.
Evidence Base

Academic References

  1. [1]
    Arvat E, et al. (1997). Stimulatory effect of adrenal androgens on the GH-releasing activity of GHRP-2 in humans. J Clin Endocrinol Metab. 82(7):2239–45. PubMed ↗
  2. [2]
    Bowers CY. (1998). Growth hormone-releasing peptide (GHRP). Cell Mol Life Sci. 54(12):1316–29. PubMed ↗
  3. [3]
    Nass R, et al. (2008). Effects of an oral ghrelin mimetic on body composition in healthy older adults. Ann Intern Med. 149(9):601–11. PubMed ↗
  4. [4]
    Veldhuis JD, et al. (1997). Dual defects in pulsatile GH secretion and clearance subserve the hyposomatotropism of obesity. J Clin Endocrinol Metab. 80(12):3532–8. PubMed ↗
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