Oral growth hormone secretagogue (GHS): non-peptide

MK-677 (Ibutamoren)

MK-677 (ibutamoren) is a non-peptide, orally active growth hormone secretagogue developed by Merck that mimics ghrelin to stimulate GH and IGF-1 release. It is not FDA-approved for any indication; Merck discontinued clinical development. Despite multiple published Phase 2 trials showing IGF-1 increases, the compound is sold as a research chemical and is widely discussed in fitness and anti-aging communities.

Evidence review Last reviewed Jul 1, 2026 Next review Jul 29, 2026
White MK-677 capsule bottle beside three capsules and a closed archive folder

Evidence snapshot

MK-677 is an oral, non-peptide ghrelin receptor agonist (GHS) developed by Merck; multiple Phase 2 trials published in peer-reviewed journals demonstrated sustained increases in IGF-1 levels.

A 12-month Phase 2 study in hip fracture recovery (NCT01016781; PMID 12004295) showed MK-677 improved functional status in elderly patients with hip fracture, but development was not advanced to approval.

A study published in the Journal of Clinical Endocrinology & Metabolism (PMID 10674575) demonstrated that oral MK-677 replicated the pulsatile GH profile seen with intravenous GH secretagogues in healthy older adults.

MK-677 is not FDA-approved for any indication and is widely sold online as a 'research chemical' or 'SARM' despite not being a SARM; FDA warning letters have addressed such marketing.

Research record

What the evidence record says

MK-677 (ibutamoren) is a non-peptide, orally active growth hormone secretagogue developed by Merck that mimics ghrelin to stimulate GH and IGF-1 release. It is not FDA-approved for any indication; Merck discontinued clinical development. Despite multiple published Phase 2 trials showing IGF-1 increases, the compound is sold as a research chemical and is widely discussed in fitness and anti-aging communities.

Evidence grade
Not Graded
Regulatory status
MK-677 (Ibutamoren) regulatory status has not been fully reviewed by Peptide Report editorial team. See company profiles and regulatory watch for current status.

Evidence records

Studies, registries, reviews, and regulatory records

Evidence timeline

What changed, and when

  1. Peptide Report last reviewed MK-677 (Ibutamoren) on 2026-07-01.

    Records: Oral Ghrelin Mimetic MK-677 Stimulates Pulsatile GH Secretion

Direct answers

Frequently asked questions

What is MK-677 (Ibutamoren)?

MK-677 (Ibutamoren) is a oral growth hormone secretagogue (ghs): non-peptide tracked by Peptide Report. See the full profile for current editorial assessment.

Open research questions

What is still unknown

  • What is the complete human evidence base for MK-677 (Ibutamoren)?
  • What are the long-term safety considerations for MK-677 (Ibutamoren)?

Tracked claims

MK-677 is widely sold online as a 'research chemical' despite having clinical trial data.

Evidence level: Community discussion

Sources: Warning Letter: Gram Peptides

How to read this: The research-chemical marketing of MK-677 exists alongside genuine Phase 2 clinical data: this creates a misleading impression of legitimacy. Track the marketing claims and FDA enforcement context.

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Sources on this page

Each source record is linked to the claim or evidence note it supports.

Oral Ghrelin Mimetic MK-677 Stimulates Pulsatile GH Secretion

Journal of Clinical Endocrinology & Metabolism (PubMed) · Peer reviewed · Feb 1, 2000 · accessed Jul 1, 2026

Svensson et al. (2000) study (PMID 10674575) demonstrating that oral MK-677 replicated the pulsatile GH profile seen with IV secretagogues in healthy older adults, with sustained IGF-1 increases over 4 weeks.

5 linked pagesOpen original · pubmed-mk677-gh-profile-2000

A 12-Month Study of the GH-Releasing Compound MK-677 in Hip Fracture Recovery

Journal of the American Geriatrics Society (PubMed) · Peer reviewed · Mar 1, 2002 · accessed Jul 1, 2026

Bach et al. (2002) 12-month Phase 2 trial (PMID 12004295) showing MK-677 improved functional status in elderly patients with hip fracture. Despite positive pharmacodynamic data, Merck did not advance MK-677 to FDA approval.

5 linked pagesOpen original · pubmed-mk677-hip-fracture-2002

MK-677 Hip Fracture Recovery Trial: ClinicalTrials.gov

ClinicalTrials.gov / U.S. National Library of Medicine · Primary regulatory · Nov 1, 2009 · accessed Jul 1, 2026

ClinicalTrials.gov registry entry (NCT01016781) for the MK-677 hip fracture recovery trial sponsored by Merck. MK-677 is not FDA-approved for any indication.

5 linked pagesOpen original · clinicaltrials-gov-mk677-hip-fracture

Warning Letter: Gram Peptides

U.S. Food and Drug Administration · Primary regulatory · Mar 31, 2026 · accessed Jun 30, 2026

FDA warning letter discussing peptide products marketed online and the limits of research-use-only positioning.

35 linked pagesOpen original · fda-gram-peptides-warning-2026

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