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.
- • MK-677 (ibutamoren) is an oral ghrelin-receptor agonist that raises GH and IGF-1 — not a peptide, not a SARM.
- • Real human data exists (Merck program) but the program was discontinued; never approved.
- • Real side-effect profile: appetite, water retention, raised fasting glucose / lower insulin sensitivity, a CHF signal in vulnerable groups.
- • Oral → no reconstitution. WADA-banned (S2). This page is honest facts + tracking, not a dose protocol.
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:
- Strong appetite increase — expected from a ghrelin-receptor agonist; the most consistently reported effect.
- Water retention / edema and swelling, sometimes lethargy or fatigue.
- Higher fasting blood glucose and reduced insulin sensitivity — clinically demonstrated (Nass 2008); relevant for anyone with prediabetes or diabetes, and a reason fasting glucose/HbA1c monitoring is sensible.
- Raised IGF-1, with a theoretical (not demonstrated) proliferative concern from chronic elevation.
- Congestive-heart-failure risk signal in older/vulnerable populations — the reason a trial was stopped early, and a concern the FDA has cited.
Tracking MK-677 in OptiPin
If you are tracking an oral GH-axis compound, OptiPin treats it like any other entry — without endorsing it:
- Daily oral dose log + reminders — record the once-daily dose and get reminded on the due day (no injection-site rotation needed — it's oral).
- IGF-1 & glucose tracking — log bloodwork (IGF-1, fasting glucose, HbA1c) over your dose timeline; given the demonstrated insulin-sensitivity effect, this is the monitoring that actually matters here.
- Weight & appetite notes — log weight and appetite over time, since increased appetite and water weight are the two most predictable effects.
- OptiInsight analysis — OptiPin's AI reads the full record (doses, labs, weight, symptoms) and surfaces what moved with what.
- Supply tracking — log the bottle/quantity; OptiPin estimates how long it lasts and warns before you run out.
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.
Download on the App StoreFAQ
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.
Sources
- Nass et al. — "Effects of an Oral Ghrelin Mimetic on Body Composition and Clinical Outcomes in Healthy Older Adults" (Annals of Internal Medicine, 2008)
- Ibutamoren — drug monograph (classification, mechanism, ~4–6 h half-life, Phase 2 status)
- DoD Operation Supplement Safety (OPSS) — MK-677 (Ibutamoren)
- Citeline/Scrip — Merck's MK-677 fails in Alzheimer's Phase II
- WADA S2 — peptide hormones, growth factors & related substances (GH secretagogues)
Related
Ipamorelin + CJC-1295 · BPC-157 · TB-500 · Peptides guide · Half-life visualizer · Bloodwork