Head to head

MK-677 vs Tesofensine

GH secretagogueMetabolic

Matching appetite control scores that point opposite ways — plus the dose, kinetics and evidence side by side.

Verdict

Same score, opposite directions

Both are weighted for appetite control, but a weight measures force, not direction: MK-677 moves it the wrong way for anyone chasing appetite control, and Tesofensine moves it the right way. Which one you want is settled by direction, not by the matching score.

What you are actually choosing between

These sit in different classes. MK-677 is a growth hormone secretagogue; Tesofensine is a metabolic compound. They get compared because of where they overlap, not because they are interchangeable.

The overlap is appetite control. On this site's goal weighting — an editorial priority score, not a measure of effect size — MK-677 rates 5/5 for appetite control and Tesofensine rates 5/5. Outside that overlap they diverge: MK-677 also carries weight for recovery and sleep and muscle growth, Tesofensine for fat loss.

One trap on this pairing: both score highly for appetite control, but they push it in opposite directions. MK-677 is flagged in this dataset as moving it the wrong way, while Tesofensine carries no such flag. A goal weight measures how hard a compound acts on something, not which way it acts — so this is the one place on the page where a tie is not a tie.

The evidence

Tesofensine sits one step firmer: approval from a regulator somewhere, though not a current FDA or EMA label — approved in Mexico at 0.5 mg; the 1 mg arm was clearly worse tolerated. MK-677 has controlled human trials behind it, without an approval — never approved, and trials flagged higher fasting glucose. One tier is a real difference but not a decisive one; it should not on its own settle the choice.

How they differ in practice

The kinetics are roughly 9× apart — 9.2 days for Tesofensine against 24 h for MK-677 — and yet both are dosed once daily. That schedule is convention rather than clearance, which is worth knowing before you assume the two behave the same way between doses.

Committed time differs: MK-677 runs 16 weeks, Tesofensine runs 24 weeks.

Risk and difficulty

The contraindication lists are not the same: MK-677 flags active malignancy, which Tesofensine does not. If any of those describe you they remove a compound from consideration outright, regardless of everything above.

MK-677 is rated intermediate here and Tesofensine advanced. That rating is about how much can go wrong in handling, dosing and monitoring, not about how well either works.

Source notes

What the evidence actually says

Verbatim, so you can check the verdict above against what it was built from.

MK-677 (Ibutamoren)

Orally active, long-acting ghrelin receptor (GHS-R1a) agonist that raises GH and IGF-1 for around 24 hours per dose. It has been through multiple human trials, including a two-year study in older adults, but was never approved for any indication and trials also flagged increased fasting glucose and reduced insulin sensitivity. It is a non-peptide small molecule, so it is taken by mouth rather than injected.

Tesofensine

An oral triple monoamine (noradrenaline, dopamine, serotonin) reuptake inhibitor, not a peptide. A 24-week randomized phase 2 obesity trial tested 0.25, 0.5 and 1.0 mg daily; 0.5 mg is the dose carried forward and the strength approved in Mexico. It is NOT FDA or EMA approved. The 1.0 mg arm produced clearly more cardiovascular and psychiatric adverse effects, so the upper end of this range is documented but not recommended. Values here are capsule strengths in mg, not vial sizes, and the reconstitution fields do not apply to an oral drug.

Side by side

The numbers

MK-677 compared with Tesofensine
AttributeMK-677Tesofensine
ClassGH secretagogueMetabolic
RoutesOralOral
Dose range10 mg–25 mg (typical 15 mg)250 mcg–1 mg (typical 500 mcg)
FrequencyOnce dailyOnce daily
Half-life24 h9.2 days
Cycle length16 weeks24 weeks
ExperienceIntermediateAdvanced
EvidenceControlled human trialsApproved elsewhere
Contraindications
  • Pregnant / nursing
  • Active malignancy
  • Under 18
  • Pregnant / nursing
  • Under 18
Side effects
  • Pronounced increase in appetite, often within the first few days
  • Water retention, puffiness in the face and ankles, and rapid scale weight gain
  • Raised fasting blood glucose and reduced insulin sensitivity — a real concern for anyone prediabetic or diabetic, and worth monitoring with bloodwork on longer runs
  • Lethargy or grogginess the morning after a pre-bed dose
  • Numbness or tingling in the hands, sometimes carpal-tunnel-like
  • Vivid dreams and deeper but occasionally disrupted sleep
  • Mild joint aches at higher doses
  • Insomnia, especially when taken late in the day
  • Dry mouth
  • Raised heart rate and blood pressure, dose-dependent and pronounced above 0.5 mg
  • Agitation, anxiety or mood change
  • Nausea and constipation

Goals

Where they overlap, and where they do not

GoalMK-677Tesofensine
appetite control
MK-677: 5/5
Tesofensine: 5/5
recovery and sleepone only
MK-677: 5/5
Tesofensine:
fat lossone only
MK-677:
Tesofensine: 4/5
muscle growthone only
MK-677: 4/5
Tesofensine:
injury repairone only
MK-677: 2/5
Tesofensine:
longevityone only
MK-677: 2/5
Tesofensine:
skin and hairone only
MK-677: 2/5
Tesofensine:

They overlap on 1 goal and diverge on 6. Weights are this site’s editorial priority score out of 5 — how central a goal is to why people use a compound. They are not effect sizes and two 5s do not mean two equal results.

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Educational information only, not medical advice. Talk to a licensed clinician before starting, changing, or stopping anything.