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.
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

Mechanism of Action

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.

Research Summary

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

Dosing Information

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

Oral GH secretagogue. Can cause water retention, increased appetite, and blood sugar issues. Some cycle it, others run year-round.

Research Dosing

Scientific studies

Doses from research studies

Duration

8-12 weeks or longer

Administration

Oral

Timing & Administration

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.

Possible Side Effects

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
  • NOT FDA approved - FDA issuing warning letters (2025)

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.

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), engineered for a long duration of action. The form most people mean by CJC-1295 includes a Drug Affinity Complex (DAC) that binds blood albumin to extend its half-life to roughly 6 to 8 days, raising GH and IGF-I for days from a single injection. It was developed by ConjuChem, reached Phase II trials and was abandoned; it is not an approved drug and is sold only as a research chemical. A version without DAC (Modified GRF 1-29) acts for only about 30 minutes.

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

Tesamorelin

FDA

Tesamorelin is a stabilized analog of growth-hormone-releasing hormone (GHRH 1-44) with a chemical modification that protects it from rapid breakdown. It is FDA-approved (brand name Egrifta) to reduce excess visceral abdominal fat in people with HIV-associated lipodystrophy, which makes it one of the few growth-hormone-axis peptides with a real approval behind it. Its evidence base is solid for that specific population and thinner for the general anti-aging and fat-loss uses it gets promoted for online.

Growth Hormone

Sermorelin

Preclinical

Sermorelin is a 29-amino-acid fragment of human growth hormone-releasing hormone (GHRH), and it is the shortest piece of GHRH that still works fully. It asks the pituitary to make and release its own growth hormone rather than injecting GH itself. It was once an FDA-approved drug for diagnosing and treating growth hormone deficiency in children, but the manufacturer pulled it from the market in 2008, so today it is available mainly through compounding pharmacies for off-label use.

Growth Hormone

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