GHRP-2 (Pralmorelin / KP-102)
GHRP-2 is a synthetic hexapeptide ghrelin mimetic that triggers growth hormone release through the GHS-R1a receptor. It produces the strongest acute GH stimulation of any GHRP. Approved in Japan as a diagnostic agent for GH deficiency. A 2005 JCEM study showed it increased food intake by 35.9% and GH output by 13x versus placebo.
FormBlends Peptide Context
Reviewed May 14, 2026Read Ghrp 2 peptide guide with the practical follow-up in mind. If the topic involves peptide therapy, the next useful step is usually to verify evidence strength, access rules, pharmacy pathway, total cost, and the personal safety details that only a clinician can review.
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Clinical decision snapshot
GHRP-2 authority snapshot
GHRP-2 is evaluated by mechanism, evidence quality, regulatory status, practical access, and safety questions a licensed clinician would need to review before use.
Evidence signal
Meaningful evidence with limits
Regulatory reality
Expected to remain Category 2 (restricted from compounding)
Safety screen
Moderate appetite increase (~36% in clinical study), Cortisol elevation of 25-35% (transient, returns to baseline in 2-3 hours), Prolactin elevation of 15-25% (transient, dose-dependent) should be reviewed in context.
This page currently connects to 5 source-backed evidence items through visible references or structured citation data.
Decision path
What is the supervised-review path for GHRP-2?
GHRP-2 should be evaluated by evidence quality, safety status, source quality, dosing context, and whether the goal fits a legitimate clinical pathway. This page is a research and decision aid, not a self-prescribing guide.
- Peptide
- GHRP-2
- Category
- Growth Hormone
- Evidence
- Meaningful evidence with limits
- FDA status
- Not FDA approved
Step 1
Check evidence level
GHRP-2 has solid human data for GH stimulation and is approved diagnostically in Japan. Reiter et al. (JCEM 2005, PMID: 15699539) showed GHRP-2 increased food intake by 35.9% and GH AUC by 13x in healthy men. Combined GHRP-2 + GHRH produced a 54-fold GH increase. The cortisol and prolactin elevation is well-characterized (Bowers et al., Eur J Endocrinol 1997).
Review evidenceStep 2
Screen safety context
Moderate appetite increase (~36% in clinical study), Cortisol elevation of 25-35% (transient, returns to baseline in 2-3 hours), Prolactin elevation of 15-25% (transient, dose-dependent) should be discussed in light of history, dose, and source.
Check side effectsStep 3
Confirm access route
If FormBlends offers access, review the product page and provider pathway before deciding.
Review product accessLast updated: April 6, 2026
Typical Dosage
100-300 mcg subcutaneous injection, 1-3 times daily on an empty stomach. The saturation dose is approximately 100 mcg (1 mcg/kg). Peak GH occurs 15-30 minutes post-injection.
Administration
Subcutaneous injection, Intranasal (lower bioavailability)
Typical Cost
$20-50 per 5 mg vial (research); $100-250/month compounded
FDA Status
Not FDA Approved
Half-Life
Approximately 25 minutes (plasma elimination). GH pulse lasts about 60 minutes.
Onset of Action
Peak GH concentration at 15 minutes post-SC injection. GH returns to baseline by 120 minutes.
Bioavailability
High via subcutaneous injection. Less than 1% orally. Variable intranasally.
About GHRP-2
GHRP-2 (Growth Hormone Releasing Peptide-2) is a synthetic hexapeptide with the sequence D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2. Its CAS number is 158861-67-7, and its molecular weight is 817.97 Da. It's the most potent GHRP for acute GH stimulation, but that potency comes with baggage. Unlike ipamorelin (which cleanly releases GH with almost no cortisol or prolactin effects), GHRP-2 raises cortisol by 25-35% and prolactin by 15-25% within 30 minutes of injection. Both return to baseline in 2-3 hours, but the elevation matters for people on long-term protocols. The appetite effect is real and measurable. Reiter et al. published a controlled study in the Journal of Clinical Endocrinology and Metabolism (2005, PMID: 15699539) showing that GHRP-2 infusion increased food intake by 35.9% in healthy men. This is less than GHRP-6 (which causes intense hunger) but more than ipamorelin (which barely affects appetite). For people trying to gain weight during recovery from illness or cachexia, the appetite boost is a feature. For people cutting, it's a problem. The synergy with GHRH analogs is where GHRP-2 gets interesting. GHRPs and GHRH work through completely different signaling pathways (Gq/11 versus cAMP). When you combine them, the GH output isn't additive, it's multiplicative. One study measured a 54-fold increase in pulsatile GH secretion with GHRP + GHRH versus baseline. This is why the classic peptide stack pairs a GHRP (like GHRP-2) with a GHRH analog (like CJC-1295 or sermorelin). In Japan, GHRP-2 is approved as a diagnostic agent for growth hormone deficiency under the brand name marketed by Kaken Pharmaceutical. A GH response below 9 ng/mL indicates adult GHD, and below 16 ng/mL indicates pediatric GHD. The regulatory situation in the US is not favorable. GHRP-2 was placed on the FDA Category 2 restricted list, and it was specifically excluded from the 14 peptides returning to Category 1 under the February 2026 HHS announcement. The cortisol and prolactin elevation were cited as safety concerns. Ipamorelin, which has none of these issues, was included in the Category 1 return. This regulatory gap has made ipamorelin the preferred clinical GHRP for most practitioners. The standard subcutaneous dose is 100-300 mcg per injection, 1-3 times daily on an empty stomach. Above about 200 mcg per injection, you hit diminishing returns on GH release while side effects continue to increase. Most protocols dose at 100 mcg (roughly 1 mcg/kg) per injection, which sits at the saturation point for GH stimulation.
How GHRP-2 Works
GHRP-2 binds the growth hormone secretagogue receptor 1a (GHS-R1a) on pituitary somatotroph cells. Unlike GHRH (which works through cAMP), GHRP-2 activates Gq/11 signaling, triggering phospholipase C activation, IP3 generation, and intracellular calcium mobilization that drives GH exocytosis. It also amplifies endogenous GHRH release at the hypothalamic level and partially counteracts somatostatin inhibition. When combined with GHRH, the result is a 54-fold increase in pulsatile GH secretion versus baseline.
Receptor targets:
Benefits
- Strongest acute GH stimulation of any GHRP
- 54-fold GH increase when combined with GHRH analogs
- Approved diagnostic agent for GH deficiency in Japan
- Increases food intake by 35.9% (useful for wasting conditions)
- GH response does not decline with age in elderly subjects
What Does the Research Say?
GHRP-2 has solid human data for GH stimulation and is approved diagnostically in Japan. Reiter et al. (JCEM 2005, PMID: 15699539) showed GHRP-2 increased food intake by 35.9% and GH AUC by 13x in healthy men. Combined GHRP-2 + GHRH produced a 54-fold GH increase. The cortisol and prolactin elevation is well-characterized (Bowers et al., Eur J Endocrinol 1997).
Growth Hormone Releasing Peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men
Journal of Clinical Endocrinology and Metabolism, 2005 · DOI · PubMed
GHRP-2 infusion at 1 mcg/kg/h increased food intake by 35.9% and GH AUC by approximately 13x versus saline in 7 healthy men
Effects of GHRP-2 and hexarelin on GH, prolactin, ACTH and cortisol levels in man
European Journal of Endocrinology, 1997 · PubMed
Characterized the dose-dependent cortisol and prolactin elevation profiles of GHRP-2 compared to GHRH and TRH stimulation
PubMed evidence trail
Research sources used to frame this page
For GHRP-2, FormBlends checks the page topic against primary trials, systematic reviews, guidelines, and current PubMed-indexed literature where available. These citations are context, not a claim that every study applies to every patient.
Ipamorelin, the first selective growth hormone secretagogue
Background source for ipamorelin selectivity and GH-secretagogue mechanism.
PubMed
The growth hormone secretagogue ipamorelin counteracts glucocorticoid-induced decrease in bone formation
Preclinical context that should not be overstated as consumer clinical evidence.
PubMed
Potential Side Effects
- Moderate appetite increase (~36% in clinical study)
- Cortisol elevation of 25-35% (transient, returns to baseline in 2-3 hours)
- Prolactin elevation of 15-25% (transient, dose-dependent)
- Water retention (mild, temporary)
- Injection site redness
- Decreased insulin sensitivity at higher doses
Drug Interactions
| Compound | Interaction | Severity |
|---|---|---|
| Somatostatin analogs (octreotide) | Directly antagonize GH release, blunting GHRP-2 effect completely. | major |
| Insulin and oral hypoglycemics | GH elevation can transiently decrease insulin sensitivity. Monitor glucose in diabetic patients. | moderate |
| GHRH analogs (sermorelin, CJC-1295) | Synergistic. Combined use produces up to 54-fold GH increase. Intentional stacking protocol, but amplifies side effects too. | moderate |
Who Is GHRP-2 For?
Women
GHRP-2 is more stimulatory than GHRH for GH release in women. No differences in response based on menstrual cycle phase. Same cortisol and prolactin elevation applies.
Adults Over 50
GH responses to GHRPs do not decline in late adulthood. Combined GHRH + GHRP-2 produced strong GH responses in elderly subjects, suggesting age-related GH decline is functional and potentially reversible.
Athletes
Prohibited at all times by WADA under S2 (Peptide Hormones, Growth Factors). Detectable via LC-MS/MS in urine. Strict liability applies.
Regulatory Status
FDA Approved
No
Compounding Legal
No
2026 HHS Status
Expected to remain Category 2 (restricted from compounding)
GHRP-2 was placed on the FDA Category 2 list and is expected to remain restricted. It was specifically excluded from the 14 peptides returning to Category 1 under the February 2026 HHS announcement, due to cortisol and prolactin elevation concerns.
Last verified: 2026-04-06
Stacking Options
GHRP-2 is commonly stacked with the following peptides for enhanced results:
Conditions Addressed
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