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This entry is not a peptide · It is included because this compound is commonly discussed alongside peptide research.

MK-677

Also known as: Ibutamoren, Nutrobal, L-163,191

At a glance

PeptiGuide dataset · reviewed Aug 2026

What it is

Oral ibutamoren compound studied for ghrelin-linked GH and IGF-1 signaling

Status

Clinical Trials

Typical dose

10–25mg

Researched for

Muscle building, sleep improvement, appetite increase

Trial progress

  1. PrePreclinical
  2. IPhase I
  3. IIPhase II
  4. IIIPhase III
  5. IVPhase IV
  6. FDAFDA approved

Phase II - Emerging human evidence with important limitations

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  • MK-677, also known as ibutamoren, is identified by the source as an oral non- ghrelin-receptor rather than a peptide.
  • The source reports human-trial evidence involving growth hormone and IGF-1 effects.
  • It is listed as not FDA approved, with investigational Phase II history and source-noted safety concerns.
  • Source-reported dosing commonly centers on 10-25 mg daily by mouth.
  • Research areas listed by the source include muscle building, sleep improvement, and appetite increase.

MK-677 is described as a selective GHS-R1a . By engaging this ghrelin-associated receptor in growth-hormone regulatory pathways, it can increase growth-hormone signaling and raise IGF-1. The source also links its ghrelin-like activity to appetite effects and notes possible cortisol changes.

Where the research stands

The source describes a mixed human-research picture. In older healthy adults, a one-year randomized study using 25 mg daily was reported to raise IGF-1 and increase fat-free mass, while strength or functional outcomes were not characterized as strong and early weight change was partly attributed to water. In an Alzheimer's disease trial with 563 participants over 12 months, IGF-1 increased but cognitive decline was not slowed. The source consistently flags appetite increase, fluid retention, and reduced insulin sensitivity as recurring tolerability concerns, and notes that the compound remains unapproved.

What it shows

Human studies

Emerging human evidence with important limitations

Limitations

Study protocols describe research and are not dosing recommendations.

Bottom line: Investigational; Phase II trials reported halted for safety concerns, with source-noted FDA enforcement activity in 2025-2026. Not FDA Approved

Typical dosing

Community

10–25 mg

daily

10 mg50 mg

Community-reported dosing only. The source notes potential water retention, appetite increase, and blood-glucose concerns, and says usage patterns vary. · Oral

Research dosing

Study-specific protocols

Doses observed in studies

10-25 mg daily

Clinical Trial Data - Investigational - Phase II trials completed

Study protocols describe research and are not dosing recommendations.

Duration
8-12 weeks or longer
Administration
Oral

Best time to take

Before bed

Once daily, consistently at the same time

Food recommendation

With or without food

Why this timing?

The source favors evening use because hunger and drowsiness may occur, and because the compound is discussed in relation to sleep-associated growth-hormone patterns.

Not everyone experiences these. Individual responses vary with dose, duration, and personal factors.

  • Increased appetite and hunger
  • Weight gain
  • Water retention or edema
  • Insulin resistance
  • Elevated blood glucose or hyperglycemia
  • Anxiety
  • Muscle or joint pain
  • Numbness or tingling
  • Heart failure risk concern
  • Possible negative impact on bone mineral density
  • Not FDA approved with FDA warning-letter context

Not everyone experiences side effects, and severity can vary by context, purity, route, and individual health factors.

One open dataset

Every fact on this page - doses, side effects, references - comes from the same PeptiGuide dataset that powers the Tracker, Compare, and the Lab.

Browse the dataset

Educational resource, not medical advice. Talk to your clinician before acting on anything here.

Community discussion

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