Research CompoundOral · Non-Peptide

MK-677

Ibutamoren — GH Secretagogue

Half-life
~24 hours
Route
Oral
Typical dose
12.5–25 mg/day
Reconstitutable
No — oral only

What is MK-677?

MK-677 (Ibutamoren) is a non-peptide growth hormone secretagogue that mimics ghrelin by binding to GHS-R1a receptors in the pituitary and hypothalamus. Unlike injectable GHRPs, it is orally bioavailable with a half-life of approximately 24 hours — allowing once-daily oral dosing.

MK-677 stimulates GH and IGF-1 release through the ghrelin receptor pathway without affecting cortisol, prolactin, or other pituitary hormones at standard doses. It produces a sustained elevation in GH pulse amplitude throughout the day.

Research Evidence

SilverIGF-1 Elevation

Multiple clinical trials in elderly and GH-deficient patients show consistent IGF-1 elevation of 40-60% at 25mg/day. Effects are dose-dependent and sustained with continued use.

SilverLean Mass & Bone Density

Studies in elderly populations demonstrate improvements in lean body mass, bone mineral density, and functional measures over 12-24 month protocols.

BronzeSleep Quality

MK-677 increases slow-wave sleep duration, which correlates with the natural GH peak. Improved sleep is consistently self-reported in community protocols.

Evidence grades: Gold = RCT human data · Silver = multiple animal studies, consistent · Bronze = limited or preliminary

Dosing Protocols

Standard dose
12.5–25 mg/day
Start at 12.5mg to assess tolerance. Most protocols use 25mg. Higher doses increase side effects without proportional GH benefit.
Timing
Before bed
Aligns with natural GH secretion peak. Reduces appetite-stimulating effects during waking hours.
Cycle length
8–16 weeks
Some protocols run continuously. Cycling 16 weeks on, 4-8 weeks off is common.

Reconstitution Guide

This compound does not require reconstitution — it is taken orally and does not require preparation.

Frequently Asked Questions

Does MK-677 suppress testosterone?

No. MK-677 acts through the ghrelin receptor and does not affect the HPT axis. It does not suppress testosterone and does not require post-cycle therapy.

What are the main side effects of MK-677?

The most common are increased appetite, water retention in the first 2-4 weeks, and fatigue at higher doses. These are dose-dependent and typically resolve with dose reduction. Transient insulin resistance has been observed at 25mg in clinical studies.

References

  1. [1]Chapman IM, Bach MA, Van Cauter E, et al. Stimulation of the growth hormone (GH)-insulin-like growth factor I axis by daily oral administration of a GH secretogogue (MK-677) in healthy elderly subjects. J Clin Endocrinol Metab. 1996;81(12):4249-4257.
  2. [2]Nass R, Pezzoli SS, Oliveri MC, et al. Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults. Ann Intern Med. 2008;149(9):601-611.
Disclaimer: This profile is for informational and research purposes only. Not medical advice. Always consult a licensed healthcare provider before using any compound.

This profile was prepared using AI-assisted research synthesis. Citations are provided where applicable — verify with primary sources before clinical application.

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