Peptides: GHRP-2 Overview

Category: growth-hormone Updated: 2026-04-04

GHRP-2 stimulates pulsatile GH release at 100mcg; cortisol and prolactin elevation are dose-dependent above 300mcg. Evidence grade B from human pharmacodynamic trials.

Key Data Points
MeasureValueUnitNotes
Evidence GradeBgradeHuman dose-finding and pharmacodynamic studies exist (PMID 11238505; 15138487); no RCTs for body composition outcomes
Standard Dose100–300mcg/injection2–3× daily; pulsatile dosing to mimic natural GH pulse pattern; do not exceed 300mcg per injection without compelling reason
GH Pulse at 100mcg~4–5×above baselineApproximate GH pulse amplitude increase at 100mcg IV/subcut dose; varies by individual baseline GH status and age
IGF-1 Elevation Onset1–2daysMeasurable serum IGF-1 elevation typically detectable within 1–2 days of regular GHRP-2 use; peak at ~7 days
Cortisol/Prolactin Threshold300mcgDose-dependent cortisol and prolactin elevation becomes clinically significant above 300mcg; stay at or below this threshold
SequenceD-Ala-D-βNal-Ala-Trp-D-Phe-Lys-NH2hexapeptide6 amino acid synthetic hexapeptide with D-amino acids at positions 1 and 2 for protease resistance
Preferred StackCJC-1295 no-DACcombinationCombining GHRP-2 with CJC-1295 no-DAC (Mod GRF 1-29) produces 3–4× greater GH pulse than GHRP-2 alone

GHRP-2 (D-Ala-D-βNal-Ala-Trp-D-Phe-Lys-NH2) is a synthetic hexapeptide growth hormone secretagogue that acts as an agonist at GHSR-1a (the ghrelin receptor). It was developed as part of the GHRP class following Bowers’ foundational work on enkephalin-derived GH-releasing peptides in the 1980s. GHRP-2 is distinguished from GHRP-6 by its greater receptor selectivity for the GH-releasing aspect of GHSR activation, with proportionally less activation of the orexigenic (appetite) pathway at equivalent doses (PMID 15138487).

Human pharmacodynamic data confirms GHRP-2 stimulates robust GH pulses at doses of 100–300mcg. IGF-1 elevation is detectable within 1–2 days of regular use, with peak elevation typically occurring by day 7 of consistent twice- or thrice-daily dosing (PMID 28859227).

GHRP-2 vs GHRP-6 vs Ipamorelin: Comparison

CharacteristicGHRP-2GHRP-6Ipamorelin
Receptor selectivityModerate — GHSR with partial orexigenicLow — broad ghrelin mimicryHigh — GHSR GH-specific, minimal appetite
GH pulse amplitude at 100mcg~4–5× baseline~4–5× baseline~3–4× baseline
Hunger stimulation (scale 1–5)2/54/51/5
Cortisol increase at 100mcgMildMildMinimal
Prolactin increase at 100mcgMildMildMinimal
Water retentionModerateModerateMild
Cortisol/prolactin at 300mcg+SignificantSignificantMild-moderate
Evidence gradeBBB

Dosing and Timing Protocol

Standard GHRP-2 protocol: 100–300mcg per injection, 2–3 times daily. Inject subcutaneously in the fasted state — at minimum 2 hours post-meal. Most effective injection windows:

  1. Pre-sleep (optimal): Aligns with the largest natural GH pulse ~60 minutes after sleep onset
  2. Fasted morning: Before breakfast, typically 8–12 hours post-last-meal
  3. Pre-workout fasted: 30–60 minutes before training on an empty stomach

Avoid injecting post-workout in a fed or high-insulin state — insulin elevation sharply blunts GHRP-2 GH response.

JurisdictionStatusScheduleNotes
USAResearch chemicalUnscheduledNot FDA-approved; WADA prohibited (S2) for competitive athletes
UKNot scheduledNoneLegal to possess; WADA prohibited under UKAD anti-doping rules
AustraliaPrescription restrictedSchedule 4 (TGA)ASADA prohibited; requires prescription; not commercially available
CanadaGray marketNo scheduleNo approved DIN; WADA prohibited for athletes
EUGenerally unscheduledVaries by countryNo EMA approval; WADA prohibited for athletes in all member states

Side Effect Profile

At standard doses (100–200mcg), GHRP-2 is generally well-tolerated. The most common side effects are:

  • Water retention: From elevated IGF-1 and GH; typically mild at standard doses
  • Hunger: Mild; less pronounced than GHRP-6 at equivalent doses
  • Cortisol/prolactin elevation: Minimal at 100mcg; becomes clinically relevant above 300mcg
  • Tingling or flushing: Brief, injection-site or systemic; not harmful

Chronic HPA axis stimulation (cortisol) from high-dose GHRP-2 is a theoretical concern for long-term use but has not been systematically studied in humans at performance protocol doses (PMID 28859227).

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Frequently Asked Questions

How does GHRP-2 compare to ipamorelin for a first-time user?

Ipamorelin is generally considered more beginner-friendly due to its highly selective GH stimulation profile with minimal cortisol and prolactin elevation at standard doses. GHRP-2 is effective but carries a measurable dose-dependent cortisol and prolactin increase, particularly above 200mcg. For users sensitive to cortisol elevation — or those managing stress response — ipamorelin is often preferred as a starting point.

Should GHRP-2 always be combined with a GHRH analogue?

Not strictly required, but the combination is recommended by most practitioners for maximal GH pulse amplitude. GHRP-2 alone at 100–300mcg produces a meaningful GH pulse. Adding CJC-1295 no-DAC (100–200mcg at the same time) produces approximately 3–4× the GH pulse via dual receptor stimulation. The combination also reduces the proportional cortisol increase relative to GH achieved.

What happens if GHRP-2 is taken with food?

Insulin and elevated blood glucose increase somatostatin tone, which blunts the GH-releasing response to GHRP-2. Studies suggest GH pulse amplitude can be reduced by 50–75% when injected in a fed versus fasted state. GHRP-2 should be injected at least 2 hours after the last meal, and food should not be consumed for at least 30–60 minutes after injection for maximal effect.

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