Educational reference only. Not medical advice. Consult a healthcare provider before starting any protocol.

Library

MK-677 (Ibutamoren)

Ibutamoren Mesylate (MK-0677, L-163,191)

MuscleFat lossSleepTissue repairHormone

What it is

A non-peptide, orally active small molecule that acts as a potent agonist of the growth hormone secretagogue receptor (GHS-R1a), mimicking endogenous ghrelin to stimulate pulsatile GH and IGF-1 release. MK-677 has been studied in multiple human randomized controlled trials across indications including sarcopenia, diet-induced catabolism, Alzheimer's disease, hip fracture recovery, and sleep quality, but has not received FDA approval for any indication. It is discussed in biohacking communities in the context of GH optimization, body composition, sleep improvement, and recovery, and is notable for its oral bioavailability and ~24-hour effective half-life.

Community-reported ranges

Ranges sourced from published clinical trial protocols, community forums, and peptide education sites. Not dosing guidance.

Reported dose range

1000025000 mcg

Estimated half-life

~24 hours (effective/biological)

Source: clinical trial dosing protocols (Nass et al. 2008; Copinschi et al. 1997)

Reported cycle length

816 weeks on

4-8 weeks off

Route

oral

Common vial sizes

10mg capsules, 25mg capsules, 25mg/mL liquid

Reported timing

Before bedtime (to align with nocturnal GH pulses and mitigate daytime appetite increase)

Reported frequency

1x daily (oral)

Frequently discussed alongside

Based on community forum discussions. Not a recommendation to combine compounds.

Published research

MK-677 has been evaluated in multiple human RCTs: a 2-year sarcopenia trial in healthy older adults (Nass et al. 2008, PMID 18981485, n=65), diet-induced catabolism reversal (Murphy et al. 1998, PMID 9467534), a large Alzheimer's trial (Sevigny et al. 2008, PMID 19015485, n=563), hip fracture recovery (Adunsky et al. 2011, PMID 21067829, terminated early), and sleep quality improvement (Copinschi et al. 1997, PMID 9349662). Key findings include sustained GH/IGF-1 elevation with oral once-daily dosing, increased lean mass, but also insulin resistance and glucose intolerance concerns with extended use. Lumos Pharma's Phase 2 OraGrowtH trials for pediatric GHD have met primary endpoints. Community dosing ranges are derived from clinical trial protocols.

Reported side effects

From community self-reports. Not from controlled studies.

From clinical trial data (Nass et al. 2008, 2-year RCT): increased appetite (most common, subsiding over months), transient lower-extremity edema, muscle pain, elevated fasting blood glucose (~0.3 mmol/L increase), decreased insulin sensitivity, weight gain (2.7 kg vs 0.8 kg placebo at 12 months), increased cortisol. A congestive heart failure safety signal led to early termination of the hip fracture trial (Adunsky et al. 2011). A case report documented hepatotoxicity (transaminitis) after 2 months of use. Community users have reported intense hunger, water retention/bloating, lethargy, numbness/tingling in extremities, vivid dreams, and joint pain.

Regulatory status

FDA (United States)

Not approved for any indication. Investigational New Drug. Received FDA Orphan Drug Designation for GH deficiency (June 2017). A hip fracture trial was terminated early due to a congestive heart failure safety signal (Adunsky et al. 2011). FDA has issued warning letters to companies marketing MK-677 products. Not eligible for pharmacy compounding — reviewed at October 29, 2024 PCAC meeting; FDA recommended exclusion from 503A bulk substances.

Health Canada

Not authorized as a therapeutic product. No DIN assigned.

WADA (Competitive Athletes)

Prohibited at all times under S2.2.4 — Growth Hormone Releasing Factors. Specifically named: 'growth hormone secretagogues (GHS) and their mimetics [e.g. anamorelin, capromorelin, ibutamoren (MK-677), ipamorelin…].' Classified as Specified Substance. Confirmed on 2025 and 2026 WADA Prohibited Lists.

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