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Peptide Profile

MK-677

Ibutamoren · MK-0677 · Nutrobal

MK-677 (ibutamoren; ibutamoren mesylate) is an orally active, non-peptide small-molecule ghrelin receptor (GHS-R1a) agonist developed by Merck as a research compound for GH deficiency and muscle-wasting conditions, notable as one…

GH / IGF AxisUnder clinical reviewResearch Only
Used forfat lossperformancelongevitycognitive
Half-life
24 hours
Routes
oral

Educational research information — not medical advice. Review primary sources and consult a qualified professional before any decision.

Educational research tools — not medical advice.

Overview

What MK-677 is

About MK-677

MK-677 mimics the action of ghrelin by binding to and activating the GHSR-1a receptor in the pituitary gland, stimulating pulsatile GH release. Its oral bioavailability distinguishes it from peptide-based GH secretagogues and its prolonged half-life results in sustained IGF-1 elevation. Research protocols have explored its effects on lean body mass, bone mineral density, and sleep architecture.

MK-677 (ibutamoren; ibutamoren mesylate) is an orally active, non-peptide small-molecule ghrelin receptor (GHS-R1a) agonist developed by Merck as a research compound for GH deficiency and muscle-wasting conditions, notable as one of the few GH secretagogues with confirmed oral bioavailability and a substantial human clinical dataset spanning multiple Phase 2 randomized controlled trials. MK-677 mimics ghrelin to stimulate pulsatile GH and IGF-1 secretion from the pituitary in a dose-dependent manner without directly replacing GH, and RCTs have demonstrated significant increases in fat-free mass and GH secretion in obese adults and in hemodialysis patients with nutritional deficits, establishing the pharmacology of oral GHS-R1a agonism in humans. Despite robust human pharmacological evidence, MK-677 was not advanced to FDA registration; Merck Phase 3 trials showed efficacy on surrogate endpoints but did not demonstrate the clinical outcomes required for approval, commercial development was discontinued, and no approved indication exists. MK-677 is a non-peptide research compound — not a peptide in the pharmacological sense — with no FDA approval; it is widely available through research chemical suppliers and used off-label, and considerations including its documented effects on insulin sensitivity, fasting glucose, and sustained IGF-1 elevation are relevant to its risk profile. MK-677 dosage in clinical trials: published RCTs studied oral doses of 10 mg, 25 mg, and 50 mg once daily. The timing of administration relative to sleep has been explored in some studies in relation to the natural nocturnal GH peak. MK-677's oral bioavailability is a practical distinction from injectable GH secretagogues — it is administered as a tablet or capsule without the reconstitution steps required for peptide injectables. Side effects documented in RCTs include increased appetite (a direct ghrelin-mimetic effect), mild peripheral edema from water retention, and transient increases in fasting blood glucose — a clinically relevant finding for individuals with pre-existing insulin sensitivity concerns. Sustained IGF-1 elevation from long-duration use is a differentiated risk characteristic compared to short-half-life injectable GHRPs. MK-677 is sometimes grouped with performance peptides due to overlapping research contexts but is pharmacologically a non-peptide small molecule. Licensed telehealth and anti-aging providers who carry growth hormone secretagogues are listed in the PeptideBase directory.

MK-677 Benefits & Research Areas

oral GH and IGF-1 stimulation without injectionfat-free mass increase documented in RCTsappetite stimulation via ghrelin receptor agonismsustained IGF-1 elevation — long-duration monitoring relevant

Research Signals

Commonly researched in the context of

High Training LoadPoor SleepSedentary

Population research notes

18–2930s40s

These signals reflect research interest areas, not treatment indications.

Pharmacokinetics

MK-677 half-life calculator

Compound & timing

Half-lifefrom PeptideBase data
Source: "24 hours" · MK-677 (PeptideBase)
to show amount remaining
24 h
0%25%50%75%100%0255075100125time since dose (h)
Plasma decay curve for MK-677: 50% remaining at 24 h after the dose.
plasma level
50%remaining in plasmaat 24 h after the dose
Half-life
24 h
~97% cleared after
5 days

Model: single-dose, first-order (single-compartment) estimate. Real clearance is multi-compartment and varies by individual and route.

The Research

What the evidence says about MK-677

Research Evidence

based on 2 studies · 2 RCTs · most recent 2018

Regulatory Status

Availability Status
Research Only
FDA Status
Under clinical review

Non-peptide ghrelin mimetic. Active IND; Phase 2/3 trials by Merck/Helsinn. Never FDA-approved. FDA enforcement actions against MK-677 supplements as unapproved new drug. Investigational only.

Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research Sources

2 sources cited · 2 strong

2 RCTs

  • Oral ghrelin receptor agonist MK-0677 increases serum insulin-like growth factor 1 in hemodialysis patients: a randomized blinded study

    Nephrology, Dialysis, Transplantation · 2018

    Research in a 3-month randomized crossover trial found that oral MK-0677 produced a 65% greater increase in serum IGF-1 compared with placebo in hemodialysis patients, with no serious adverse effects, providing evidence for the GH secretagogue pathway as a potential approach to protein-energy wasting in chronic kidney disease.

    RCTn=22StrongPMID 28340044
  • Two-month treatment of obese subjects with the oral growth hormone (GH) secretagogue MK-677 increases GH secretion, fat-free mass, and energy expenditure

    Journal of Clinical Endocrinology and Metabolism · 1998

    Research in an 8-week randomized placebo-controlled trial found that oral MK-677 25 mg daily increased serum IGF-I by approximately 40%, significantly increased fat-free mass as measured by dual-energy X-ray absorptiometry, and transiently increased basal metabolic rate in obese men, without significant changes in total or visceral fat.

    RCTn=24StrongPMID 9467542

MK-677 Side Effects & Safety Considerations

No FDA-approved label for this compound. Cautions below are extrapolated from its mechanism/drug class — investigational; educational only.

Warnings & cautions

Active malignancy — caution (raises GH/IGF-1)Pregnancy — cautionUncontrolled diabetes / insulin resistance (can raise fasting glucose)Known hypersensitivity

Class-based (investigational)

Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.

Certificates of Analysis

2 COAs on record for MK-677

PeptideBase reports these lab-published figures and does not itself test, endorse, or certify any product. Confirmed by lab results were matched against the issuing laboratory's own records — either the lab served the document, or its own hosted copy matches ours byte for byte. For every other result the badge states what is known about the lab: that it can be checked and no result is recorded yet, that it can't be checked, or that we have not reviewed it.

PeptideBase provides educational research tools and provider discovery. It does not provide medical advice, diagnosis, treatment, prescribing guidance, or dosing instructions. Consult a qualified healthcare professional before making health decisions.

Community Experience

What people report about MK-677

n=14early data

Self-reported, anecdotal experiences aggregated from public Reddit discussions — community sentiment, not clinical evidence or medical advice.

Outcome distribution

36%improved
Improved
5 · 36%
Mixed
5 · 36%
No clear effect
2 · 14%
Worse
2 · 14%

Side effects people mention

Counts are mentions across reports, not incidence rates.

Decreased appetite2
Vivid dreams2
Water retention2
Elevated heart rate1

Most reported

What they wish they'd known

  • Longer durations of consistent use were emphasized as necessary before judging effectiveness.3×thread 1thread 2thread 3
  • Blood sugar and hormonal effects surprised users who had not anticipated metabolic disruption.3×thread 1thread 2thread 3
  • Some expected physical outcomes, such as height changes, simply did not materialize.2×thread 1thread 2
  • Water retention was less severe than many anticipated, and was often manageable.2×thread 1thread 2

Based on 14 community reports · Updated

Frequently Asked Questions — MK-677

MK-677 (ibutamoren; ibutamoren mesylate) is an orally active, non-peptide small-molecule ghrelin receptor (GHS-R1a) agonist developed by Merck as a research compound for GH deficiency and muscle-wasting conditions, notable as one of the few GH secretagogues with confirmed oral bioavailability and a substantial human clinical dataset spanning multiple Phase 2 randomized controlled trials. MK-677 mimics ghrelin to stimulate pulsatile GH and IGF-1 secretion from the pituitary in a dose-dependent manner without directly replacing GH, and RCTs have demonstrated significant increases in fat-free mass and GH secretion in obese adults and in hemodialysis patients with nutritional deficits, establishing the pharmacology of oral GHS-R1a agonism in humans.

oral GH and IGF-1 stimulation without injection, fat-free mass increase documented in RCTs, appetite stimulation via ghrelin receptor agonism, sustained IGF-1 elevation — long-duration monitoring relevant.

Research on MK-677 primarily documents effects related to oral GH and IGF-1 stimulation without injection and fat-free mass increase documented in RCTs and appetite stimulation via ghrelin receptor agonism and sustained IGF-1 elevation — long-duration monitoring relevant. These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.

Reported contraindications and considerations for MK-677 include Active malignancy — caution (raises GH/IGF-1), Pregnancy — caution, Uncontrolled diabetes / insulin resistance (can raise fasting glucose). 1 additional consideration are noted in the safety profile above. This is educational information only — consult a qualified healthcare professional before use.

For MK-677, it is designated for research use only. Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

47 providers in the directory currently offer MK-677.

Research in a 3-month randomized crossover trial found that oral MK-0677 produced a 65% greater increase in serum IGF-1 compared with placebo in hemodialysis patients, with no serious adverse effects, providing evidence for the GH secretagogue pathway as a potential approach to protein-energy wasting in chronic kidney disease.

MK-677 is featured in the following research stacks on PeptideBase: MK-677 + Epithalon: Sleep Architecture & Anti-Aging.

Access

How to get MK-677

Where to buy MK-677

47 providers
36 Clinics3 Telehealth8 Online Vendors63 in stock

Research stacks

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Commonly stacked with

Questions to ask your provider

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