Peptide guides
What is GHRP-2 (Pralmorelin)? What it does, benefits and what the evidence shows
A ghrelin-receptor peptide developed at Tulane University and Polygen. It is approved in Japan as a diagnostic for growth hormone deficiency, and that is the whole approved story. Here is what the human studies show about everything else, and what independent lab reports show (nothing yet).

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Key facts
- GHRP-2, also called pralmorelin, mimics ghrelin; Japan's regulator lists it as GHRP Kaken 100, a one-time injection to diagnose growth hormone secretion deficiency, on sale since February 2005.
- After GHRP-2, peak growth hormone averaged about 1 microgram per liter in 58 patients with severe deficiency versus about 85 in 77 healthy people (Chihara et al., 2007).
- In seven lean healthy men, a GHRP-2 infusion raised food intake at a buffet meal by about 36% compared with saline (Laferrère et al., 2005).
- FDA lists GHRP-2 among bulk drug substances that may present significant safety risks for compounding (503B, injectable and nasal routes), added September 29, 2023.
- We found no controlled human trial of GHRP-2 for muscle growth, fat loss, recovery or aging; the muscle-protection findings come from cultured cells and the anti-inflammatory findings from arthritic rats.
- As of September 29, 2026, VendorVerify's database contained no lab results for GHRP-2.
GHRP-2, also known by its drug name pralmorelin, is a synthetic peptide that mimics ghrelin and prompts the pituitary to release a large burst of growth hormone. It has one approved use that we could find: in Japan, as an injection given once to help diagnose growth hormone deficiency. It is not approved anywhere we could find as a treatment, and the claims that sell it on the grey market (muscle, fat loss, recovery, anti-aging) have no controlled human trial behind them.
What GHRP-2 is and how it works
GHRP-2 is one of a series of small growth hormone-releasing peptides developed by Polygen in Germany and by Cyril Bowers's group at Tulane University in the US. These compounds mimic ghrelin, the 28-amino-acid hormone that regulates growth hormone release (Adis drug profile, Drugs in R&D, 2004). The Kaken Pharmaceutical company later held the marketing rights to it, and in the same profile it is listed under the name pralmorelin and under the code KP-102.
Like other GHRPs, it doesn't supply growth hormone itself; it prompts the pituitary to release its own. That means it depends on a pituitary that still responds. In eleven adults with isolated growth hormone deficiency caused by a mutated GHRH receptor, GHRP-2 raised growth hormone about 4.5-fold, versus about 79-fold in normal controls; the authors concluded that GHRP-2 works partly on the pituitary directly, without needing the GHRH signal (Gondo et al., Journal of Clinical Endocrinology & Metabolism, 2001).
The approved use is a diagnostic test
Japan's drug regulator, PMDA, lists a single-use injection called GHRP Kaken 100 (in Japanese, 注射用GHRP科研100), containing pralmorelin hydrochloride. Its indication is "the diagnosis of growth hormone secretion deficiency" (成長ホルモン分泌不全症の診断), sales began in February 2005, and the package insert was revised most recently in July 2025 (PMDA package insert). The insert contraindicates use in pregnancy and lists a heat sensation (16.0% of cases), low blood pressure, nausea, dizziness, facial flushing and small lab changes among its adverse reactions.
How the test works: in healthy people GHRP-2 produces a big growth hormone spike, while in people with growth hormone deficiency the spike is much smaller. The 2004 Adis profile said a threshold peak of 15 micrograms per liter separated patients from healthy controls (Adis, 2004). The same 2004 profile said a US phase II program for growth hormone deficiency with Wyeth appeared to have been discontinued, and that a Japanese short-stature program was then in phase II; we found no later approval for either.
That is the whole approved story: a one-off test, in one country, not a treatment. A 2019 forensic-chemistry paper summarizes it the same way, noting that of all the GHRPs developed as drug candidates, only GHRP-2 has received a clinical approval (Popławska and Błażewicz, Drug Testing and Analysis, 2019).
What people use it for
| Claimed benefit | Evidence | Source |
|---|---|---|
| Diagnosing growth hormone deficiency (one-time test) | Approved use (Japan only, diagnostic only) | PMDA package insert |
| Short-term growth hormone release | Human trials | Chihara et al., European Journal of Endocrinology, 2007 |
| Increased appetite and food intake | Early human data | Laferrère et al., 2005 |
| Restarting the growth hormone axis in prolonged critical illness | Early human data | Van den Berghe et al., Clinical Endocrinology, 2002 |
| Protecting muscle from breakdown, calming inflammation | Animal/lab only | Yamamoto et al., 2008 (muscle cells); Granado et al., 2005 (arthritic rats) |
| Muscle growth, fat loss, recovery, anti-aging | Anecdotal | none |
What the research actually shows
Growth hormone release and the diagnostic test
The diagnostic case is the best-tested part. In a validation study of 77 healthy people and 58 patients with severe growth hormone deficiency (defined by the standard insulin tolerance test), the peak growth hormone response to a single intravenous GHRP-2 injection was far lower in patients (about 1 microgram per liter) than in healthy people (about 85). Repeat tests were reproducible, results were only mildly affected by age and adiposity, and a cut-off of 15 micrograms per liter corresponded to the 3 microgram cut-off used for the insulin test (Chihara et al., European Journal of Endocrinology, 2007). A Japanese comparison in 71 patients with pituitary tumors judged the GHRP-2 test an acceptable alternative to the insulin tolerance test, though the authors noted that criteria should be adjusted to each population (Endocrine Journal, 2013). In 56 children, the test correlated with the insulin tolerance test and took an hour or less (Journal of Pediatric Endocrinology & Metabolism, 2010).
There are limits. In a retrospective study of 23 adolescents, two patients passed the GHRP-2 cut-off but failed other tests, and the authors suggested the cut-off may miss some deficient patients (Journal of Pediatric Endocrinology & Metabolism, 2024). A test that produces a big, reliable spike is a good diagnostic; it is not evidence that the spike does anything for you.
The test isn't only about growth hormone. GHRP-2 also stimulates ACTH, the pituitary signal that drives cortisol. In six patients with hypothalamic or pituitary disorders, GHRP-2 produced significant ACTH release, which the authors read as evidence of direct ACTH-releasing activity (Kimura et al., Endocrine Journal, 2010). If you have seen GHRP-2 compared with ipamorelin, this off-target hormone effect is the usual contrast; see our ipamorelin guide and the sibling hexarelin guide, which describes similar cortisol and prolactin effects.
Appetite
GHRP-2 does what ghrelin does to hunger. In seven lean, healthy men given a GHRP-2 infusion versus saline, then offered a buffet meal, every man ate more on GHRP-2; average intake rose about 36% (Laferrère et al., Journal of Clinical Endocrinology & Metabolism, 2005). That is a tiny, short study, but a consistent one, and it is probably the most reliable non-diagnostic effect on record. It also helps explain why GHRP-2 shows up in conversations about weight gain, and why it is a poor fit for anyone who wants the opposite.
Prolonged critical illness
A small randomized study in 33 men with prolonged critical illness tested a short course of placebo, GHRP-2 alone, GHRP-2 with TRH, or GHRP-2 with TRH and pulsed GnRH. GHRP-2 alone reactivated growth hormone secretion and normalized IGF-I and related proteins. But the metabolic benefits the authors were after (reduced ureagenesis, higher osteocalcin) appeared only with the combined regimens, and by the end of the course GHRP-2 alone raised lactate and white blood cell counts (Van den Berghe et al., 2002). This is intensive-care research at a small scale, and it says nothing about healthy people.
Repeated use
Whether the response fades with repeated dosing is less clear for GHRP-2 than for its sibling hexarelin. In a 1996 report, Bowers and Granda-Ayala found that whether the growth hormone response becomes desensitized during chronic GHRP-2 administration depends partly on the dosage and frequency (Journal of Pediatric Endocrinology & Metabolism, 1996). That study didn't report muscle or fat outcomes in its abstract.
Muscle, fat loss, recovery and anti-aging
We found no controlled human trial of GHRP-2 for muscle growth, fat loss, recovery or aging. The muscle-protection findings are from cultured muscle cells (Yamamoto et al., Life Sciences, 2008) and the anti-inflammatory findings from arthritic rats (Granado et al., AJP Endocrinology & Metabolism, 2005). Those are hypotheses, not results in people.
Side effects and risks
The approved diagnostic is a single injection given under medical supervision, so its safety data doesn't translate to repeated self-administered use. What we can say:
- The label. The Japanese insert lists a heat sensation (16.0% of cases), low blood pressure, nausea, dizziness, facial flushing, raised ALT and higher white blood cell counts, and contraindicates use in pregnancy (PMDA).
- FDA's view. GHRP-2 is on FDA's list of bulk drug substances with significant safety risks for compounding (503B), added September 29, 2023. FDA cites potential immunogenicity from aggregation and peptide-related impurities, notes GHRP-2 contains an unnatural amino acid that complicates characterization, and says it is aware of reports of serious adverse events in patients who received it, including increased insulin requirement, death of critically ill study subjects, infection and pancreatitis, though causality has not been established (FDA, Category 2 bulk drug substances, page current as of April 22, 2026). Those are FDA's words, not confirmed harms.
- Off-target hormones and appetite. ACTH release (Kimura et al., 2010) and a marked rise in food intake (Laferrère et al., 2005).
- No long-term data. We found no long-term safety study in healthy adults.
- Sport. GHRP-2 (pralmorelin) is named on the 2026 WADA Prohibited List, in the growth hormone-releasing peptide class, prohibited at all times (WADA Prohibited List 2026).
There is also a documented quality problem in this corner of the market. GHRP-2 has been identified and quantified in tablets sold as an over-the-counter nutritional supplement (Thomas et al., Drug Testing and Analysis, 2010), and a modified glycine analogue of GHRP-2 was identified in a seized injection vial (Popławska and Błażewicz, 2019). Neither tells you how common such products are, but both say a vial's label is not proof of what is inside.
What the lab tests show
As of September 29, 2026, VendorVerify's database has no lab results for GHRP-2. That doesn't mean the vials are good or bad; it means no report has been submitted that we can count. If you have had a GHRP-2 vial tested, submitting the report is the fastest way to change that.
Because we don't have enough lab data on this compound to rank vendors for it, here are the highest-ranked vendors across all compounds right now. A vendor's overall record is a signal, not a guarantee for a compound they have never had tested.
Highest-ranked peptide vendors right now
Live from independent lab reports, mostly paid for by buyers. Only vendors with 5+ reports are ranked. Updates as new reports come in.
| # | Vendor | Verdict | Score | Failed vials | Lab reports | Dose vs label |
|---|---|---|---|---|---|---|
| 1 | BFF/AMO | Above market | 96.7 | 0.7% | 185 | +2.9% |
| 2 | ZLZ | Above market | 91.8 | 0.0% | 14 | +7.2% |
| 3 | QST | Above market | 91.0 | 0.0% | 13 | +6.9% |
| 4 | Uther | Above market | 90.9 | 0.0% | 45 | +10.2% |
| 5 | TCI | Above market | 90.1 | 0.0% | 72 | +9.3% |
A strong record describes vials people tested, not a guarantee for yours. Test your own vial when you can.
Full vendor ratingsBuying smarter
With no compound-specific data, lean on the general checks. Look at each vendor's full record and how many reports sit behind the score. Treat a vendor-posted COA as a starting point (how to read a peptide COA, fake peptide COAs). Paying for identity, purity and quantity testing on your own vial is worth it for a compound with no track record in our data; how to get a peptide tested walks through it, and endotoxin in research peptides covers when to add that test.
If a report comes back with a fail, stop using that batch, tell anyone who bought from the same run, bring the report to the vendor, and submit it to VendorVerify. Buyers who research GHRP-2 often also look at hexarelin, ipamorelin, sermorelin and CJC-1295; the peptide hub lists every compound we track.
Database figures are from VendorVerify as of September 29, 2026. This isn't medical advice; GHRP-2 sold outside a licensed setting is unregulated and sold for research use only, and its only approval we could find is a Japanese one-time diagnostic.
Figures in this article come from the lab results on VendorVerify as of Sep 29, 2026. The vendor and peptide pages always show the latest numbers.
Frequently asked questions
What does GHRP-2 do?
It mimics ghrelin and prompts the pituitary to release a large, short burst of growth hormone; it also stimulates ACTH and increases appetite in human studies. Its only approved use we could find is as a one-time diagnostic test for growth hormone deficiency in Japan.
What are the benefits of GHRP-2?
The proven ones are a growth hormone spike (which makes it a workable diagnostic test) and increased appetite in small studies. No controlled human trial shows muscle gain, fat loss or anti-aging benefits.
Is GHRP-2 the same as pralmorelin?
Yes. Pralmorelin is the drug name for GHRP-2, also coded KP-102. The Japanese diagnostic product is GHRP Kaken 100, which contains pralmorelin hydrochloride.
Is GHRP-2 approved anywhere?
Japan's regulator lists it as a diagnostic injection for growth hormone secretion deficiency, on sale since February 2005. We found no approval for it as a treatment, and no approval from other regulators; a US treatment program was reported as apparently discontinued in 2004.
Is GHRP-2 safe?
Not enough is known for repeated use. The diagnostic label lists a heat sensation, low blood pressure, nausea and dizziness, and FDA lists GHRP-2 among substances with significant safety risks for compounding, citing immunogenicity concerns and unconfirmed reports of serious adverse events. There is no long-term human safety data.
Does GHRP-2 make you hungry?
Yes, in a small study: seven lean healthy men ate about 36% more at a buffet while on a GHRP-2 infusion than on saline, matching what ghrelin does.
What is the difference between GHRP-2 and ipamorelin?
Both trigger a growth hormone pulse by acting on ghrelin receptors. GHRP-2 also stimulates ACTH in human studies, while ipamorelin has been described as more selective in lab work. Only GHRP-2 has an approval we could find, and it is for a diagnostic test. See our [ipamorelin guide](/blog/what-is-ipamorelin).


