For laboratory and research use only. Not for human consumption.
Growth Hormone

GHRP-6

Also known as: Growth Hormone Releasing Peptide 6, SKF-110679

Clinical Trials
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Key Facts: GHRP-6

Category
Growth Hormone
FDA Status
Not FDA Approved
Clinical Status
Preclinical/Investigational - FDA Category 2 (restricted from compounding; expected to remain restricted after 2026 reclassification due to cortisol/prolactin concerns)
Banned in Sport (WADA)
Prohibited at all times under WADA S2 (GH-releasing peptides), named on the list.
Administration
Subcutaneous injection, ideally fasted
Typical Dose
100-300 mcg 2-3x daily
Frequency
2-3x daily
Duration
8-12 weeks
Also Known As
Growth Hormone Releasing Peptide 6, SKF-110679

How does GHRP-6 work?

GHRP-6 binds and activates the growth hormone secretagogue receptor type 1a (GHS-R1a), the same receptor later found to be the natural target of the hunger hormone ghrelin. When it switches that receptor on in the pituitary and hypothalamus, the pituitary fires off a pulse of growth hormone. Because GHS-R1a also sits on appetite-driving neurons in the brain (the NPY/AgRP cells of the arcuate nucleus), GHRP-6 is a strong appetite stimulant, more so than the other GHRPs. At higher doses it also nudges up cortisol and prolactin, since the receptor system is not perfectly selective for the GH pathway.

What does the research show?

GHRP-6 has been studied in humans, but mostly as a lab and diagnostic probe rather than as a treatment with large clinical trials behind it. Early work in the 1980s and 1990s showed it reliably triggers growth hormone release, and chasing its mechanism is literally what led Kojima and colleagues to discover ghrelin in 1999, which reframed how we understand hunger and GH control. A 2013 pharmacokinetic study in nine healthy men found oral bioavailability under 1 percent and an elimination half-life around 2.5 hours, which is why it is given by injection. The popular claims about muscle gain, fat loss, and healing in fitness circles are not backed by controlled human outcome trials. It is not approved by the FDA or EMA for any use and remains a research chemical, with appetite stimulation, water retention, and cortisol/prolactin bumps as known effects.

Trial Progress:Preclinical
Pre
I
II
III
IV
FDA

What doses have been studied?

Human Trials·Human studies conducted, not FDA approved

Typical Dosingⓘ

Community experience

Common Dose

100-300 mcg 2-3x daily

Range

100-500 mcg per dose

Frequency

2-3x daily

Reported effects include a marked increase in hunger. Reported protocols administer in a fasted state, and research contexts include appetite stimulation and growth hormone release.

Research Dosingⓘ

Scientific studies

Doses observed in research studies

Duration

8-12 weeks

Administration

Subcutaneous injection, ideally fasted

When and how is GHRP-6 taken?

Best Time to Take

Before bed or morning (fasted)

2-3 times daily, 30 min before meals or before bed

Food Recommendation

Take on empty stomach

Why This Timing?

GHRP-6 stimulates GH release and increases appetite. Take fasted for maximum GH response. Evening dose supports natural nighttime GH surge.

What are the side effects of GHRP-6?

Not everyone experiences these effects. Individual responses vary based on dosage, duration, and personal factors.

  • ●Significant hunger increase (most pronounced of all GHRPs)
  • ●Water retention
  • ●Elevated cortisol levels
  • ●Elevated prolactin levels
  • ●Flushing
  • ●Nausea
  • ●Headache
  • ●May trigger histamine release - use caution with MCAS or histamine sensitivity
  • ●Limited long-term safety data

References

Research This Peptide Further

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Frequently Asked Questions

What does GHRP-6 do?

GHRP-6 is a synthetic six-amino-acid peptide (His-D-Trp-Ala-Trp-D-Phe-Lys-NH2) that tricks the body into releasing its own growth hormone. It was one of the first growth hormone secretagogues ever made, and the hunt to find out why it worked led scientists straight to the discovery of ghrelin. It has no approval as a drug anywhere and is used only as a research compound.

How does GHRP-6 work?

GHRP-6 binds and activates the growth hormone secretagogue receptor type 1a (GHS-R1a), the same receptor later found to be the natural target of the hunger hormone ghrelin. When it switches that receptor on in the pituitary and hypothalamus, the pituitary fires off a pulse of growth hormone. Because GHS-R1a also sits on appetite-driving neurons in the brain (the NPY/AgRP cells of the arcuate nucleus), GHRP-6 is a strong appetite stimulant, more so than the other GHRPs. At higher doses it also nudges up cortisol and prolactin, since the receptor system is not perfectly selective for the GH pathway.

Is GHRP-6 FDA approved?

No, GHRP-6 is not currently FDA approved. Current status: Preclinical/Investigational - FDA Category 2 (restricted from compounding; expected to remain restricted after 2026 reclassification due to cortisol/prolactin concerns)

Is GHRP-6 banned in sport?

Prohibited at all times under WADA S2 (GH-releasing peptides), named on the list.

What are the side effects of GHRP-6?

Reported side effects include: Significant hunger increase (most pronounced of all GHRPs), Water retention, Elevated cortisol levels, Elevated prolactin levels, Flushing. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of GHRP-6?

Community-reported common dose: 100-300 mcg 2-3x daily (2-3x daily). Range: 100-500 mcg per dose. Administration: Subcutaneous injection, ideally fasted. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with GHRP-6 or used in similar applications.

Ipamorelin

Clinical Trials

Ipamorelin is a synthetic pentapeptide growth hormone secretagogue developed by Novo Nordisk and derived from GHRP-1. It is researched mainly for stimulating the body's own growth hormone (GH) release, and was studied in humans primarily for postoperative ileus and gut motility rather than anti-aging. It is not an approved drug anywhere: it reached Phase II trials, was discontinued for insufficient efficacy, and is now sold only as a research chemical.

Growth Hormone

GHRP-2

Clinical Trials

GHRP-2 (generic name pralmorelin) is a synthetic hexapeptide growth hormone secretagogue and a second-generation cousin of GHRP-6. It prompts the pituitary to release growth hormone and is the one peptide in this family with an actual regulatory approval: it is licensed in Japan as a diagnostic agent for growth hormone deficiency. Outside that narrow diagnostic use it has no approval and is sold elsewhere only as a research compound.

Growth Hormone

CJC-1295 (No DAC)

Clinical Trials

CJC-1295 is a synthetic analog of growth hormone-releasing hormone (GHRH), specifically a modified GHRH(1-29). The name covers two different products. CJC-1295 with DAC (Drug Affinity Complex) binds blood albumin, which stretches its half-life to roughly 6 to 8 days and raises GH and IGF-I for days from a single injection; this is the version ConjuChem took to Phase II before abandoning it, and the version the human data are about. CJC-1295 without DAC (Modified GRF 1-29, the form this page is named for) lacks the albumin tether and is much shorter acting, though its human half-life has not been formally published. Neither is an approved drug, both are sold only as research chemicals, and GHRH analogs are banned in sport by WADA.

Growth Hormone

MK-677

Clinical Trials

MK-677 (ibutamoren) is not actually a peptide, it is a small, orally active non-peptide molecule that mimics ghrelin, your hunger and growth-hormone hormone. Taken as a daily pill, it reliably pushes up growth hormone and IGF-1 levels, which is why it is popular for muscle and recovery. It has been through real human trials but was never approved as a drug, and the trials that mattered most for older adults and Alzheimer's came up short.

Growth Hormone

HGH (Somatropin)

FDA

Human growth hormone is the real thing rather than a secretagogue: a 191-amino-acid protein identical to what your pituitary makes, produced recombinantly since the 1980s. It is a properly approved medicine for growth hormone deficiency, and it is also the most misused compound in this entire space. Almost everything you read about HGH for anti-aging or physique traces back to a single small 1990 study whose own author later disowned how it was used.

Growth Hormone

IGF-1 DES

Preclinical

IGF-1 DES is insulin-like growth factor 1 with its first three amino acids chopped off, leaving a 67-residue peptide. That small cut makes it bind poorly to the IGF binding proteins that normally keep IGF-1 in check, so more of it reaches the receptor and it acts stronger, but shorter. It occurs naturally in small amounts (it was first isolated from human fetal brain tissue) and is sold online as a muscle-building research peptide. There are no human trials of it at all, so everything said about it in people is extrapolation.

Growth Hormone

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