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MK-677: ibutamoren, explained

MK-677 (ibutamoren) is an oral growth-hormone secretagogue — and, importantly, it is neither a peptide nor a SARM, despite being sold alongside both. Unlike the injectable research peptides, it actually has real human trial data — but its development was discontinued, it was never approved, and it carries a genuine side-effect profile. This page is the honest version: what it is, what the trials showed, the half-life vs the 24-hour IGF-1 elevation, the side effects worth taking seriously, the regulatory and anti-doping status, and how to track it. It is not dosing advice.

Status — as of June 2026
Unapproved. Development discontinued. WADA-banned. MK-677 is not FDA-approved for any use and is not a legal dietary-supplement ingredient. It reached Phase 2 (including an Alzheimer's trial that failed and a hip-fracture trial stopped early on a heart-failure signal) but no drug application was ever filed. The FDA has issued warning letters over bodybuilding products containing it. It is on the WADA S2 prohibited list (GH secretagogues), banned at all times. Nothing here is a recommendation to obtain or use it.
Class
Oral GH secretagogue
Target
Ghrelin receptor
Half-life
~4–6 h (oral)
Status
Research · banned in sport
TL;DR

What it is — and what it isn't

MK-677, also called ibutamoren (development code MK-0677), is an orally active, non-peptide small molecule that acts as a selective agonist at the ghrelin receptor (GHS-R) — a growth-hormone secretagogue. It mimics the hormone ghrelin to stimulate the pituitary to release GH, which in turn raises IGF-1.

Two corrections, because the market gets this wrong constantly: MK-677 is not a SARM (SARMs bind the androgen receptor; MK-677 binds the ghrelin receptor — completely different) and it is not a peptide (it's a small molecule, taken as a pill or oral liquid, not an injectable peptide). It's listed here on the peptides hub because that's where people look for it and because it's run for similar GH-axis goals — but mechanistically it stands apart.

What the trials showed

Unlike most research compounds, MK-677 has real human clinical-trial data. Merck investigated it for age-related muscle loss, hip-fracture recovery, GH deficiency and Alzheimer's. The key trial — Nass et al., 2008, Annals of Internal Medicine (2-year, randomized, placebo-controlled; 65 healthy adults aged 60–81, 25 mg/day) — found 24-hour GH rose ~1.8-fold and IGF-1 ~1.5-fold (restored toward young-adult levels), with fat-free mass up ~1.1 kg over 12 months. Crucially, there was no improvement in strength or physical function, and insulin sensitivity declined (fasting glucose up, HbA1c up ~0.2%).

The honest, load-bearing part: the development program was discontinued. An Alzheimer's Phase 2 trial reported it was ineffective at slowing progression. A hip-fracture trial was stopped early on a safety signal — congestive heart failure in more MK-677 participants than placebo (a fluid-retention/CHF concern). It reached Phase 2, no New Drug Application was ever submitted, and it was never approved for any indication. The lean-mass biomarker story is real; the "it's a proven, safe anti-aging drug" story is not.

The numbers — half-life vs the 24-hour myth

This is the most-confused pharmacology point. MK-677 is taken orally, once daily. Its elimination half-life is short — about 4–6 hours (characterized in animals). But a single oral dose keeps IGF-1 elevated for roughly 24 hours, which is what makes once-daily dosing work.

Many vendor pages claim a "24-hour half-life" — that's incorrect. It conflates the duration of IGF-1 elevation (≈24 h, a downstream effect) with the plasma elimination half-life (≈4–6 h). The distinction matters because it changes how you think about timing and accumulation. Trials used 25 mg/day; the commonly reported range is 10–25 mg/day — presented as what's reported, not a recommendation. Because it's oral, there's no bacteriostatic-water reconstitution step the injectable peptides need; if it's sold as an oral liquid, it's dosed by milligrams of solution.

Side effects — worth taking seriously

MK-677 has a more concrete side-effect profile than most compounds in this space, which is worth stating plainly rather than glossing:

This is not a prescription, a dose, or a sourcing guide. MK-677 is an unapproved compound whose development was discontinued, with documented effects on blood glucose and a heart-failure safety signal, and it's banned in tested sport. We are not prescribers and do not recommend obtaining or using research chemicals. Discuss any GH-axis compound with a qualified clinician — especially if you have any glucose or cardiovascular history.

Tracking MK-677 in OptiPin

If you are tracking an oral GH-axis compound, OptiPin treats it like any other entry — without endorsing it:

Track it properly

Log doses, labs & weight in OptiPin

Daily reminders, IGF-1/glucose-over-dose charts, weight & appetite tracking, supply countdown, and OptiInsight analysis — all on-device. The monitoring that matters for a compound that moves your blood sugar.

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FAQ

Is MK-677 approved or legal?

No — not FDA-approved and not a legal supplement ingredient. It reached Phase 2 but no drug application was filed and development was discontinued. The FDA has warned companies selling bodybuilding products containing it. Unapproved in Germany/EU too.

Is MK-677 a SARM or a peptide?

Neither. It's an oral, non-peptide small molecule that activates the ghrelin receptor as a GH secretagogue. SARMs bind the androgen receptor; MK-677 doesn't. It's often sold alongside or mislabeled as a SARM, but it's mechanistically unrelated — and not a peptide.

What does it do to GH and IGF-1?

Raises both. In a 1-year trial, daily MK-677 increased 24-h GH ~1.8× and IGF-1 ~1.5× and added ~1.1 kg fat-free mass — but with no gain in strength or function, and reduced insulin sensitivity.

What's the half-life? Is it really 24 hours?

No. Elimination half-life is ~4–6 h (animal-characterized); IGF-1 stays elevated ~24 h, which supports once-daily oral dosing. The "24-hour half-life" claim conflates the two. Trials used 25 mg/day.

Is it banned in sport, and what are the side effects?

WADA S2 (GH secretagogues), banned at all times. Side effects: strong appetite increase, water retention, fatigue, raised fasting glucose / lower insulin sensitivity, and a CHF safety signal in older/vulnerable trial participants.

Educational only, not medical advice. MK-677 is an unapproved compound with a discontinued development program, demonstrated effects on blood glucose and a heart-failure safety signal, and it's banned in tested sport. OptiPin does not recommend obtaining or using research chemicals. Discuss any GH-axis compound with a qualified clinician.

Sources

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