MK-677 (Ibutamoren), product photo
SARMs

MK-677 (Ibutamoren)

Oral ghrelin receptor agonist. Stimulates the endogenous growth hormone axis - not a classical SARM, but typically grouped there in stack contexts.

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At a glance

MK-677 (Ibutamoren) by the numbers

The key figures from our lexicon. Drag the point along the curve to see how much is left after one dose, by calculation.

Full lexicon entry

How long does it stay in the body?

Share left after one dose, calculated with a half-life of ~24 hours

Half-life ~24 hours
After 48 hours: 25 %
Hour 24 · 50 %Hour 48 · 25 %Hour 72 · 12.5 %Hour 120 · 3.1 %

Simplified model without an absorption phase, half-life from the TPD lexicon.

Class
Ghrelin receptor agonist

GHSR, orally active

Half-life
about 24 hours
Use
Oral

1 tablet per day

Sizes
10 to 15 mg

2 sizes in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

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Knowledge

Everything about MK-677 (Ibutamoren)

Description

MK-677 (Ibutamoren, Ibutamoren Mesylate) is an oral ghrelin receptor agonist and growth hormone secretagogue. Despite being listed in the SARM category, MK-677 doesn’t act structurally or mechanistically via the androgen receptor; it activates the GHS receptor (ghrelin receptor) in the hypothalamus and pituitary.

Per study reports MK-677 stimulates pulsatile growth hormone secretion via the physiologic pathway. Unlike exogenous GH (rhGH), MK-677 preserves the natural negative feedback loop via IGF-1, preventing overstimulation. Studies show that older adults under MK-677 reach GH pulse amplitudes typical of young adults.

Pharmacokinetics are excellent: orally available with a 4-6 hour half-life. A once-daily dose suffices to elevate IGF-1 levels over 24h. Compared to GHRPs (peptide secretagogues like Ipamorelin), MK-677 is substantially more practical (oral vs subcutaneous).

In the landmark Nass 2008 study (Annals of Internal Medicine), MK-677 increased fat-free mass in older adults by 1.6 kg vs placebo over two years. Known effects in studies include increased appetite (ghrelin action), mild fluid retention and slight increase in fasting glucose (about 5 mg/dL).

You can order MK-677 as oral tablets in one bottle with 10mg or 25mg per tablet.

This information is for research and educational purposes only. No medical recommendations.

Risks & Safety

MK-677 sits in the mid range of the risk scale. As a ghrelin receptor agonist the compound acts via a physiologic pathway, but several accompanying effects are consistently documented in the studies.

Documented in studies and the literature:

  • Appetite increase: as a direct ghrelin action, a markedly increased appetite is the most commonly documented effect.
  • Water retention: mild fluid retention is described in the studies, especially at the start of use.
  • Blood sugar: a slight rise in fasting glucose is documented, relevant in pre-existing insulin resistance research.
  • Prolactin: a possible rise in prolactin levels is described in the literature.
  • No HPG suppression: unlike true SARMs, MK-677 does not suppress the HPG axis.

Monitoring via bloodwork is recommended. This classification does not replace medical advice. Risk and responsibility for any actual use lie entirely with the buyer.

Studies

Dosing

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More in the lexicon

FAQ

Frequently asked

Sources for every answer: lexicon entry

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Is ibutamoren approved?

No, as of 26 October 2026 there is no approval. ChEMBL lists phase 2 as the highest phase. The registry lists two phase 3 trials under the name LUM-201 in children with growth hormone deficiency, one recruiting, the other not yet.

How does ibutamoren work?

According to ChEMBL it binds directly to the ghrelin receptor GHSR and activates it. In older adults mean 24-hour growth hormone rose by 97 percent because existing pulses got higher, not more frequent. IGF-1 was in the range of young adults after 4 weeks.

Does ibutamoren build muscle?

Fat-free mass rose in trials: by 1.1 kg in 12 months in healthy older adults (placebo -0.5 kg). In obese men it rose within 8 weeks as well. Strength and function did not improve in the older adults, though. Part of the gain can be water.

What happens to sleep?

In a small trial with young adults the highest study dose lengthened deep sleep by about 50 percent and REM sleep by more than 20 percent. Deviations from normal sleep fell from 42 to 8 percent. In older adults REM sleep rose by almost 50 percent.

Why was there no benefit despite higher IGF-1?

In Alzheimer's IGF-1 rose by 72.9 percent while disease progression did not change. After a hip fracture IGF-1 also rose, but most function measures did not improve. The trial was stopped early because of heart failure in a few patients.

Which side effects were seen?

Most often more appetite that eased after a few months, plus mild fluid retention in the legs and muscle pain. Fasting blood sugar rose and insulin sensitivity fell. Cortisol rose slightly in the long-term trial.

How long has ibutamoren been studied in humans?

The longest trial ran 2 years in healthy older adults and confirmed the 12-month results. The Alzheimer's trial ran 12 months with 563 participants.

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