Short answer: they are different kinds of drug that happen to share a code prefix. Ostarine (MK-2866, enobosarm) is a SARM: it acts on the androgen receptor, builds a little lean mass, and lowers testosterone and HDL cholesterol. MK-677 (ibutamoren) is not a SARM: it acts on the ghrelin receptor, raises growth hormone and IGF-1, and mostly brings hunger, water retention and higher blood sugar. In trials in older adults, both added roughly 1 kg of lean or fat-free mass.

Ostarine vs MK-677 at a glance

Ostarine MK-677
What it is Selective androgen receptor modulator (SARM), nonsteroidal GH secretagogue (ghrelin receptor agonist)
Approval Not approved; furthest stage: Phase 3 Not approved; furthest stage: Phase 3
Human studies (counted in our records) 8 17
Half-life ~14–24 h Not established in humans
Testosterone suppression score 2/3 1/3
Liver risk score 2/3 1/3
Evidence score 3/3 3/3
WADA Prohibited at all times (S1.2 Other anabolic agents) Prohibited at all times (S2.2.4 Growth hormone releasing factors)
Target Androgen receptor Ghrelin (GHS) receptor; raises GH and IGF-1
Lean mass in trials +1.3 kg vs placebo in 86 days (3 mg/day, older adults) +1.1 kg vs −0.5 kg placebo over 12 months (25 mg/day, older adults)
SwissChems product Ostarine (MK-2866), (10mg/capsule), 60 Capsules MK-677 (Ibutamoren), (10mg/capsule) 60 Capsules

Scores run from 0 (none) to 3 (high); see our methodology. Data from the SARMs database.

How far Ostarine got in clinical research Furthest stage of human clinical trials reached (Preclinical = animal or cell studies only; Approved = approved as a medicine somewhere).
How far Ostarine got in clinical researchOstarine: Phase 3 (8 human studies); MK-677: Phase 3 (17 human studies)PreclinicalPhase 1Phase 2Phase 3ApprovedOstarineOstarine: Phase 3 (8 human studies)Phase 3MK-677MK-677: Phase 3 (17 human studies)Phase 3

Source: Sarmguide compound database; Ostarine: GTx, Inc. Provides Corporate Update And Reports 2013 Financial Results (press release, 4 March 2014) (2014).

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Testosterone suppression: Ostarine compared Sarmguide score from 0 (none found) to 3 (marked suppression), based on the cited studies of each compound. "(animal)" means the score rests on animal data because suppression was not measured in men; compounds with no data at all are left out. Ostarine: Yes, partly. In older men on 1–3 mg/day for 86 days, total testosterone fell by about 6–7 nmol/L vs placebo and SHBG fell on 3 mg. Free testosterone, LH and FSH did not change significantly. A 14-day Phase 1 study in healthy men (up to 30 mg/day) also found dose-dependent drops in SHBG and total testosterone, without a clinically significant change in free testosterone.
Testosterone suppression: Ostarine comparedOstarine: Moderate; MK-677: MildNone foundMildModerateMarkedOstarineOstarine: ModerateModerateMK-677MK-677: MildMild

Source: Sarmguide compound database; Ostarine: The selective androgen receptor modulator GTx-024 (enobosarm) improves lean body mass and physical function in healthy elderly men and postmenopausal women: results of a double-blind, placebo-controlled phase II trial (2011).

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How they work

Ostarine binds the androgen receptor and was designed to act more on muscle and bone than on the prostate. Because it is an androgen-receptor drug, the brain sees “enough androgen” and lowers natural testosterone. MK-677 copies the hunger hormone ghrelin: the pituitary releases more growth hormone, which raises IGF-1; in older adults, 12 months raised GH 1.8-fold and IGF-1 1.5-fold. It does not act on the androgen receptor, so it is not expected to shut down testosterone the way a SARM does.

What the trials show

Outcome Ostarine MK-677
Lean mass +1.3 kg vs placebo (86 days); +1.0–1.5 kg in cancer patients +1.1 kg vs −0.5 kg (12 months)
Fat About 0.6 kg less than placebo Total and belly fat unchanged; limb fat rose; weight +2.7 kg
Strength and function Improved on 3 mg in Phase 2; Phase 3 lung cancer trials missed their goals Strength and function unchanged
Testosterone Total testosterone −6 to −7 nmol/L vs placebo; SHBG down Small drop in total testosterone in one 8-week trial; LH and FSH unchanged
Cholesterol HDL −17% to −27% LDL down slightly
Blood sugar Insulin resistance improved (86 days) Fasting glucose up about 5 mg/dL; insulin sensitivity down
Newest research With Wegovy: 71% less lean-mass loss (company topline, 2025) Phase 3 in children with GH deficiency (as LUM-201)

Side effects

Ostarine MK-677
Lower testosterone, SHBG and HDL More appetite (67% vs 36% placebo)
Dose-dependent ALT rises; case reports of cholestatic liver injury Water retention and leg swelling; muscle and joint pain
Liver-enzyme rises at high trial doses (9–18 mg/day) in women with breast cancer Higher blood sugar; heart-failure signal in frail older adults after hip fracture

Half-life

Ostarine’s half-life is about 14–24 hours in Phase 1 studies. No human plasma half-life has been published for MK-677; the FDA found no detailed human pharmacokinetic data, and its GH effect is described as lasting about 24 hours.

Stacking ostarine and MK-677

They are often stacked because they work through different routes, but no study has tested the combination. The closest human data come from a case report of a different SARM, LGD-4033, with MK-677: over 5 weeks, testosterone fell 62%, HDL fell 36% and LDL rose 40%. Our stack checker shows the overlapping risks; see also ostarine stacks.

Neither is approved. In December 2025, FDA warning letters to an online seller named products sold as “Ostarine MK-2866” and “MK-677 Ibutamoren” as unapproved new drugs. In Australia both are prescription-only, and possession without authority is illegal. WADA bans ostarine under S1.2 (SARMs) and MK-677 under S2.2.4 (growth hormone secretagogues), at all times.


Verdict

Ostarine is the better-studied muscle compound of the two in shorter trials and has some evidence for keeping muscle during GLP-1 weight loss, at the cost of lower testosterone and HDL and rare serious liver injury. MK-677 adds weight partly as water, brings hunger and higher blood sugar, and has a heart-failure signal in frail patients, but it barely touches testosterone. Choose what to read next: ostarine before and after · MK-677 before and after · cardarine vs ostarine

Frequently asked questions

Is MK-677 the same as ostarine?

No, unrelated drugsEvidence: Human data

Ostarine (MK-2866) is a SARM that acts on the androgen receptor; MK-677 (ibutamoren) is a growth hormone secretagogue that acts on the ghrelin receptor. The similar codes do not mean they are related.

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Is MK-677 a SARM?

NoEvidence: Human data

It is a growth hormone secretagogue that copies ghrelin and does not act on the androgen receptor, though it is often sold alongside SARMs.

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Which builds more muscle, ostarine or MK-677?

About the same in trialsEvidence: Trial

In older adults, both added about 1–1.3 kg of lean or fat-free mass: ostarine over 86 days, MK-677 over 12 months. MK-677 did not improve strength.

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Does MK-677 shut down testosterone like ostarine?

Much lessEvidence: Trial

Ostarine lowered total testosterone by 6–7 nmol/L versus placebo. MK-677 caused a small drop in one 8-week trial, without changing LH or FSH.

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Can you stack ostarine and MK-677?

Never studiedEvidence: Human data

No study has tested the combination. In a case report of LGD-4033 plus MK-677, testosterone fell 62% and HDL 36% over 5 weeks.

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Which has fewer side effects?

They differEvidence: Trial

Ostarine lowers testosterone and HDL and has liver injury case reports. MK-677 increases appetite, water retention and blood sugar, with a heart-failure signal in frail older adults.

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Are ostarine and MK-677 legal?

Neither is approvedEvidence: Law

FDA warning letters in December 2025 named products sold as both as unapproved new drugs. WADA bans both at all times.

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Sources

  1. The selective androgen receptor modulator GTx-024 (enobosarm) improves lean body mass and physical function in healthy elderly men and postmenopausal women: results of a double-blind, placebo-controlled phase II trial 2011 · PMID 22031847
  2. Effects of enobosarm on muscle wasting and physical function in patients with cancer: a double-blind, randomised controlled phase 2 trial 2013 · PMID 23499390
  3. EMERALD study protocol (ISRCTN12213700, University of Liverpool, version 6.0, 2021): a window of opportunity study of enobosarm in ER+/AR+ early breast cancer 2021
  4. Veru Announces Positive Topline Data from Phase 2b QUALITY Clinical Study: Enobosarm Preserved Lean Mass in Patients Receiving WEGOVY (Semaglutide) for Weight Reduction (press release, 27 January 2025) 2025
  5. Activity and safety of enobosarm, a novel, oral, selective androgen receptor modulator, in androgen receptor-positive, oestrogen receptor-positive, and HER2-negative advanced breast cancer (Study G200802): a randomised, open-label, multicentre, multinational, parallel design, phase 2 trial 2024 · PMID 38342115
  6. Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults: a randomized trial 2008 · PMID 18981485
  7. Discrepancy between serum leptin values and total body fat in response to the oral growth hormone secretagogue MK-677 1999 · PMID 10468903
  8. FDA Briefing Document, Pharmacy Compounding Advisory Committee, 29 October 2024: Ibutamoren Mesylate 2024
  9. LGD-4033 and MK-677 use impacts body composition, circulating biomarkers, and skeletal muscle androgenic hormone and receptor content: A case report 2022 · PMID 36303408
  10. FDA Warning Letter to an online seller of products marketed as SARMs (MARCS-CMS 719257), 12 December 2025 2025
  11. Therapeutic Goods (Poisons Standard—June 2026) Instrument 2026 (F2026L00633) 2026
  12. World Anti-Doping Code International Standard: Prohibited List 2026 2025