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Growth Hormone

MK-677

Also known as: Ibutamoren, Nutrobal, L-163,191

Clinical Trials
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Key Facts: MK-677

Category
Growth Hormone
FDA Status
Not FDA Approved
Clinical Status
Investigational - Phase II trials halted (safety concerns). FDA enforcement escalated 2025-2026: product recalls, warning letters, and public safety alerts about congestive heart failure risk.
Banned in Sport (WADA)
Prohibited at all times under WADA S2 (growth hormone secretagogues), named on the list as ibutamoren (MK-677).
Administration
Oral
Typical Dose
10-25 mg daily
Frequency
Once daily, often before bed
Duration
8-12 weeks or longer
Also Known As
Ibutamoren, Nutrobal, L-163,191

How does MK-677 work?

MK-677 is a selective agonist of the growth hormone secretagogue receptor (GHS-R1a), the same receptor the hormone ghrelin binds. By activating that receptor in the pituitary and hypothalamus, it triggers pulses of growth hormone release, which in turn raises IGF-1 (insulin-like growth factor 1) from the liver. Because it copies ghrelin, it also tends to increase appetite, and it can nudge up cortisol levels too. The effect is sustained because it is long-acting and orally available, unlike injectable peptides that mimic ghrelin or growth-hormone-releasing hormone.

What does the research show?

MK-677 has unusually good human data for a compound sold in the gray market, and the data is a mix of clear wins and clear failures. In a one-year randomized trial of 65 healthy older adults (Annals of Internal Medicine, 2008), 25 mg daily raised IGF-1 and increased fat-free mass, basically lean tissue, though much of the early body-weight gain was water and the functional strength benefits were not impressive. In Alzheimer's disease, a large 563-patient, 12-month randomized trial (Neurology, 2008) confirmed it raised IGF-1 but did nothing to slow cognitive decline. Across studies the consistent downsides are increased appetite, fluid retention, and reduced insulin sensitivity (higher blood sugar). So the muscle-and-IGF-1 effect is real and well documented, but MK-677 failed its biggest disease trials, remains unapproved, and is banned in sport by WADA.

Trial Progress:Phase II
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

10-25 mg daily

Range

10-50 mg daily

Frequency

Once daily, often before bed

A non-peptide growth hormone secretagogue. Reported adverse effects include fluid retention, increased appetite and altered blood glucose. Reported schedules vary between defined courses with breaks and continuous use.

Research Dosingⓘ

Scientific studies

Doses from research studies

Duration

8-12 weeks or longer

Administration

Oral

When and how is MK-677 taken?

Best Time to Take

Before bed

Once daily, consistently at the same time

Food Recommendation

With or without food

Why This Timing?

MK-677 can cause drowsiness and hunger. Evening dosing minimizes daytime appetite increase and supports sleep-related GH release.

What are the side effects of MK-677?

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

  • ●Increased appetite and hunger
  • ●Weight gain
  • ●Water retention/edema
  • ●Insulin resistance
  • ●Elevated blood glucose/hyperglycemia
  • ●Anxiety
  • ●Muscle or joint pain
  • ●Numbness/tingling
  • ●Risk of heart failure (FDA concern - clinical trial halted)
  • ●May negatively impact bone mineral density

References

Research This Peptide Further

Frequently Asked Questions

What does MK-677 do?

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.

How does MK-677 work?

MK-677 is a selective agonist of the growth hormone secretagogue receptor (GHS-R1a), the same receptor the hormone ghrelin binds. By activating that receptor in the pituitary and hypothalamus, it triggers pulses of growth hormone release, which in turn raises IGF-1 (insulin-like growth factor 1) from the liver. Because it copies ghrelin, it also tends to increase appetite, and it can nudge up cortisol levels too. The effect is sustained because it is long-acting and orally available, unlike injectable peptides that mimic ghrelin or growth-hormone-releasing hormone.

Is MK-677 FDA approved?

No, MK-677 is not currently FDA approved. Current status: Investigational - Phase II trials halted (safety concerns). FDA enforcement escalated 2025-2026: product recalls, warning letters, and public safety alerts about congestive heart failure risk.

Is MK-677 banned in sport?

Prohibited at all times under WADA S2 (growth hormone secretagogues), named on the list as ibutamoren (MK-677).

What are the side effects of MK-677?

Reported side effects include: Increased appetite and hunger, Weight gain, Water retention/edema, Insulin resistance, Elevated blood glucose/hyperglycemia. Individual responses vary based on dosage, duration, and personal health factors.

What is the typical dose of MK-677?

Community-reported common dose: 10-25 mg daily (Once daily, often before bed). Range: 10-50 mg daily. Administration: Oral. Community-reported doses. Not medical advice. Consult healthcare provider.

Related Peptides

Peptides commonly compared with MK-677 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

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

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

GHRP-6

Clinical Trials

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.

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

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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