MK-677

Also known as: Ibutamoren, MK-0677, L-163,191

4.5 (150 reviews)

4.5

out of 5.0

A non-peptide, orally active growth hormone secretagogue that mimics ghrelin to stimulate sustained GH and IGF-1 elevation for up to 24 hours.

Research Overview

MK-677 (Ibutamoren) is a non-peptide, orally active growth hormone secretagogue developed by Merck. Although not technically a peptide, it is frequently discussed alongside GH secretagogue peptides due to its mechanism of action as a ghrelin receptor (GHS-R1a) agonist. Its oral bioavailability and long duration of action (approximately 24 hours) distinguish it from injectable peptide secretagogues.

MK-677 works by mimicking the action of ghrelin at its receptor, stimulating GH release from the pituitary while also increasing appetite through the same pathway. It produces sustained elevations in GH and IGF-1 levels without significantly altering cortisol levels. Notably, MK-677 does not suppress the natural pulsatile pattern of GH release and maintains its efficacy during chronic administration without the tolerance issues seen with some peptide secretagogues.

Extensive clinical research including Phase II trials has demonstrated that MK-677 increases GH secretion and IGF-1 levels to those of healthy young adults. Studies in elderly populations have shown improvements in sleep quality, nitrogen balance, and lean body mass. Research has also explored its potential in treating growth hormone deficiency, muscle wasting, osteoporosis, and age-related frailty.

Documented Research Effects

Dosage & Protocol

Typical Dose Range

10000 – 25000

mcg per dose

Frequency

1x daily (oral)

Cycle Length

8-16 weeks

Common Vial Sizes

25

Calculate exact draw volumes and reconstitution steps.

Use Calculator

Dosage information is for research reference only. Always follow established research protocols. Not medical advice.

Storage & Handling

Lyophilized Powder

Temperature Room temperature
Shelf Life 2+ years

Frequently Asked Questions

MK-677 (Ibutamoren) is neither a traditional peptide nor a SARM. It is a non-peptide ghrelin mimetic and growth hormone secretagogue that is taken orally. It mimics the action of ghrelin at the GHS-R1a receptor to stimulate growth hormone release. Its oral bioavailability and long half-life (~24 hours) distinguish it from injectable peptide secretagogues.

The standard dosage is 10-25 mg taken once daily, typically before bed to align with the natural GH pulse during sleep. Starting at 10 mg for the first 1-2 weeks helps assess tolerance, particularly regarding appetite stimulation and water retention. Most users settle on 15-25 mg daily for the duration of the cycle.

Yes, increased appetite is one of the most common side effects of MK-677 due to its action on ghrelin receptors. This effect is most pronounced during the first 2-4 weeks and tends to diminish somewhat with continued use. Taking MK-677 before bed rather than in the morning can help mitigate appetite-related issues during the day.

Yes, MK-677 can increase fasting blood glucose and reduce insulin sensitivity, particularly at higher doses or with long-term use. This is a known effect of elevated growth hormone levels. Monitoring fasting glucose is recommended, especially for individuals with pre-existing insulin resistance. Berberine or metformin are sometimes used alongside to manage this effect.

MK-677 cycles typically last 8-16 weeks, though some protocols extend to 6-12 months given its oral convenience. GH and IGF-1 elevations remain sustained without significant desensitization. However, longer cycles require monitoring of blood glucose and insulin sensitivity. A common approach is 3 months on followed by 1 month off.

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