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Hormones & endocrine-related compounds

Ibutamoren

Ibutamoren

Ibutamoren (MK-677) is an oral ghrelin-receptor agonist and growth-hormone secretagogue that raises GH and IGF-1 in human trials. It is better framed as an endocrine research compound than as a nootropic: Alzheimer and healthy-aging trials did not prove cognitive or functional benefit. Buyer decisions should start with sport prohibition, glucose, edema and cardiovascular safety context, and product-identity concerns.

Glucose MetabolismHormonal Axis RelatedSyntheticClinical ResearchLimited Human EvidenceEmerging ResearchPopulation Specific Evidence
Updated October 2026/7 min read/8 citations
Reviewed by the NootropicsIndex editorial team.Method: prioritize cited human research and official safety or regulatory sources; compare retailer-listed prices without endorsing products.Affiliate disclosure
01

What is it?

What it is

5

Ibutamoren, commonly sold as MK-677, is an oral non-peptide ghrelin-receptor agonist that stimulates growth hormone release and increases IGF-1. It is not a vitamin, amino acid, herb, or conventional dietary supplement ingredient in the practical buyer sense.

Evidence snapshot6
The best evidence is endocrine target engagement. That does not translate into proven memory, focus, anti-aging, recovery, or bodybuilding outcomes; the large Alzheimer trial is a useful negative anchor for cognitive claims.

Common marketplace name

1

Often sold as MK-677 or ibutamoren capsules, including by vendors that also sell SARMs or research chemicals.

Research-code variant

7

Several clinical papers use MK-0677 for ibutamoren mesylate.

Healthy-user claims are the weak link

5

The visible product market often implies rest, recovery, muscle, or anti-aging benefits. Clinical data support hormone-marker changes more strongly than real-world improvements in strength, cognition, function, or long-term health.

02

Names, aliases and forms

Common NameIbutamoren
Research CodesMK-677; MK-0677
Chemical NameIbutamoren mesylate
Regulatory NameGrowth hormone secretagogue
03

Mechanisms of action

Ghrelin-receptor agonism

5

Ibutamoren mimics ghrelin-like signaling at the growth-hormone secretagogue receptor, increasing pulsatile growth hormone secretion and downstream IGF-1 in controlled trials.

Metabolic downstream effects

8

In an eight-week trial of otherwise healthy obese men, oral MK-677 impaired glucose tolerance even though fasting glucose and insulin did not change. A normal fasting measurement therefore does not establish unchanged glucose handling.

04

Potential effects and evidence map

Human trials consistently show increased growth hormone and IGF-1, a hormone involved in growth signaling. These laboratory changes have not established a useful nootropic effect: a large Alzheimer trial found no clinical benefit, and a healthy older-adult trial found no strength or functional improvement despite increased fat-free mass. Evidence grade C reflects this limited transfer to healthy buyers, rather than uncertainty that the compound affects hormones.

Effect domainMagnitudeGrade
Physical energy / endurance5
CumulativeConfidence: Medium

Older-adult trials show GH/IGF-1 and some lean-mass signals, but strength, function, and recovery outcomes are mixed or mostly unimproved.

Note Body-composition changes do not establish improved physical performance.

0/5
C
Memory / learning6
CumulativeConfidence: Medium

A large Alzheimer trial increased IGF-1 but did not slow clinical progression, so cognition and memory claims are weak.

Note The Alzheimer trial does not establish memory benefits in healthy adults.

0/5
D
05

Typical dosages and timing

Studied adult dose525 mg once daily

Several adult trials used 25 mg/day. That clinical-study context should not be read as a general safe dose for unsupervised use.

06

Timing & effect horizon

Effect horizonCumulative
Cumulative
Study window5Cumulative
12 months
Marker changes are not outcome changes5

The healthy older-adult trial assessed its primary outcomes after 12 months, with exploratory follow-up to 2 years. This is a study window, not a recommended cycle or a duration of cognitive benefit. The reviewed sources do not establish a useful nootropic onset, acute benefit duration or a verified plasma The time for blood levels to fall by half during the final elimination phase.Source for this comparison.

07

Safety, side effects and risk profile

Why the base risk is moderate5
For identified oral ibutamoren at studied adult exposure, moderate base risk reflects clinically relevant changes in glucose handling. A low rating would understate these measured metabolic effects in otherwise healthy participants. Increased appetite, mild edema and muscle symptoms were often transient; the small trials cannot quantify serious-event risk in younger healthy adults. Heart-failure concerns in frail patients, sport rules and contaminated products are separate targeted cautions.
Legal / regulatory risk2
Confidence: High

Ibutamoren is explicitly prohibited in sport under the WADA 2026 list; anti-doping status is separate from retail availability.

Note Regulatory clinical-use varies by jurisdiction; anti-doping status is separate from supplement-store availability.

4/5
B
Hormonal caution5
Confidence: High

Human trials show meaningful GH/IGF-1 target engagement plus glucose, insulin-sensitivity and cortisol signals, so this is endocrine-active rather than benign wellness support.

Note Base-risk calibration rests on measured glucose and insulin-sensitivity changes in otherwise healthy trial participants, not on sport rules or product adulteration.

3/5
B
Cardiovascular caution3
Confidence: Medium

FDA highlights a congestive-heart-failure safety signal from a hip-fracture ibutamoren trial, and edema/fluid-retention signals are clinically relevant.

Note Score reflects fluid-retention concern at studied oral exposure. The separate serious heart-failure signal was in frail hip-fracture patients; it must not be read as a healthy-young-adult incidence estimate.

3/5
C
GI discomfort5
Confidence: Medium

Increased appetite was frequent in the older-adult study and generally subsided over several months; this is a tolerability concern, not evidence of gastrointestinal injury.

Note Increased appetite may be unwelcome when managing food intake.

1/5
C
Evidence uncertainty6
Confidence: High

The strongest evidence shows hormone-marker movement, while cognition, healthy aging, recovery, and performance outcomes remain limited, mixed, or negative.

Note The trial populations are not equivalent to self-directed retail MK-677 buyers.

4/5
C
monitoring concern5glucose, insulin sensitivity, edema

In a healthy older-adult trial, MK-677 increased fasting glucose, decreased insulin sensitivity, increased body weight, and commonly caused increased appetite plus transient mild lower-extremity edema and muscle pain.

high-priority caution7trial stopped early

A trial in older adults recovering from hip fracture stopped early after a congestive-heart-failure signal. FDA identifies this as a serious risk in certain patients; it is not an estimate of the risk in healthy young users.

do not assume purity4adulteration alerts exist

Australia's TGA found undeclared metandienone in Pharmatech MK-677 capsules in June 2026. This finding is specific to that product and does not establish adulteration in the offers displayed here.

09

Practical buying and quality notes

  • Compare capsule strength and total labeled ingredient amount before comparing unit prices: equal capsule counts do not imply equal contents. Check whether milligrams refer to ibutamoren or its mesylate salt. The current catalog includes inconsistent duplicate price records; verify package price, currency and quantity at the merchant before using any displayed minimum. Shipping and discounts can change the final cost.
  • A capsule count and milligram claim are not enough. Prefer lot-specific third-party identity testing, impurity testing, and a seller that does not frame MK-677 as a harmless dietary supplement.4
  • Hormone markers and fat-free mass are not interchangeable with strength, performance or healthy longevity. In the controlled older-adult study, additional fat-free mass did not produce improved strength or function. A product promise of those outcomes goes beyond that evidence.5
10

FAQ

Is there an evidence-based MK-677 cycle?

5

No safe self-directed cycle has been established by the cited trials. A trial observation window describes when researchers measured outcomes; it does not establish a recommended length of use or a safe break between cycles.

Is Ibutamoren the same as a SARM?

2

No. Ibutamoren is a growth-hormone secretagogue, not a selective androgen receptor modulator. It is still often sold beside SARMs and remains prohibited in sport because of its endocrine performance-enhancing pathway.

Is MK-677 a nootropic?

6

Not in the evidence-first sense. It changes GH/IGF-1 markers, but human cognition evidence is weak, and a large Alzheimer trial did not show clinical benefit despite IGF-1 increases.

Does capsule strength establish a safe dose?

5

No. Per-capsule strength describes a product, not a validated safe daily intake. A label also needs to distinguish the mesylate salt from the active compound; retail naming alone cannot resolve that difference.

What about pregnancy or combining MK-677 with medicines?

1

The cited adult trials do not establish safety during pregnancy or breastfeeding, or safe combinations with medicines and other performance-enhancing compounds. These gaps do not establish a specific interaction, but the existing glucose and fluid-retention signals make an assumption of safety inappropriate.

11

References

  1. Operation Supplement Safety (OPSS). Performance Enhancing Substance: MK-677 (Ibutamoren).
  2. World Anti-Doping Agency. The 2026 Prohibited List: International Standard.
  3. U.S. FDA. Ibutamoren mesylate safety-risk listing for compounding.
  4. Therapeutic Goods Administration. Unapproved ibutamoren capsules (MK-677) found to contain undisclosed anabolic steroid.
  5. Nass R, Pezzoli SS, Oliveri MC, Patrie JT, et al. Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults: a randomized trial. Ann Intern Med. 2008;149(9):601-611.
  6. Sevigny JJ, Ryan JM, van Dyck CH, Peng Y, et al. Growth hormone secretagogue MK-677: no clinical effect on AD progression in a randomized trial. Neurology. 2008;71(21):1702-1708.
  7. Adunsky A, Chandler J, Heyden N, Lutkiewicz J, et al. MK-0677 (ibutamoren mesylate) in patients recovering from hip fracture: a multicenter, randomized, placebo-controlled phase IIb study. Arch Gerontol Geriatr. 2011;53(2):183-189.
  8. Svensson J, et al. Two-month treatment of obese subjects with the oral growth hormone secretagogue MK-677 increases GH secretion, fat-free mass, and energy expenditure. J Clin Endocrinol Metab. 1998;83(2):362-369.
Note

This page is informational and summarizes available evidence. It is not medical advice, a recommendation, or a substitute for guidance from a qualified clinician.