All peptides
SARM

MK-2866

Also known as: Ostarine, Enobosarm, GTx-024

limited human dataWADA bannedNot FDA approvedResearch only
Mechanism of Action

MK-2866, also called enobosarm or ostarine, is a selective androgen receptor modulator studied for muscle wasting. The mechanism is androgen receptor activation with a nonsteroidal ligand, so ProtoComp should treat it as an anabolic-recovery signal while preserving liver, lipid, and endocrine caution.

Key Citations
Published Dose Range
Low10 mg/day
Typical15-25 mg/day
High25 mg/day

Most studied SARM in clinical trials — Phase 2 data for muscle wasting, cachexia, and sarcopenia. Dose-dependent HPG effects are milder than RAD-140 or LGD-4033 at low doses.

Published Cycle Range
Short4 wks
Typical8 wks
Long12 wks

Milder profile than other SARMs but not suppression-free at higher doses.

Off-cycle: 4 weeks

Administration
Routesoral
FrequencyOnce daily
Preferred timingMorning, with or without food

Half-life ~24 hours.

Safety Profile

Contraindications

  • Liver disease
  • Pregnancy
  • Prostate cancer

Common side effects

  • Mild HPG suppression (dose-dependent)
  • HDL reduction
  • Mild fatigue

Serious risks

  • HPG suppression at higher doses
  • Rare liver abnormalities in case reports

Requires monitoring

  • Liver function
  • Testosterone (males)
  • Lipid panel

Pregnancy / breastfeeding

Contraindicated

Sex-Specific Notes

Male

Mildest HPG suppression among popular SARMs but still present at ≥15 mg/day

Female

Sometimes used at lower doses by female athletes — still research-only with limited safety data

Common Misconceptions
  • Not suppression-free at typical doses
  • Not approved for human use despite multiple Phase 2 trials
Commonly Stacked With
GW-501516
  • Do not stack with other SARMs
Next Steps

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Reference information only. Always confirm with your clinician before changing your protocol.