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SARM

LGD-4033

Also known as: Ligandrol, VK5211

limited human dataWADA bannedNot FDA approvedResearch only
Mechanism of Action

LGD-4033 is a nonsteroidal selective androgen receptor modulator designed to stimulate androgen receptor signaling with tissue-selective intent. Human phase 1 data show pharmacokinetic and lean-mass signals, but long-term safety and real-world performance use remain unresolved.

Key Citations
Published Dose Range
Low2.5 mg/day
Typical5-10 mg/day
High10 mg/day

Phase 2 trials completed for muscle wasting. Dose-dependent lean mass gain and HPG suppression documented in healthy men at 1 mg/day.

Published Cycle Range
Short6 wks
Typical8 wks
Long12 wks

HPG suppression is dose-dependent but present even at 1 mg/day. Post-cycle therapy recommended.

Off-cycle: 8 weeks

Administration
Routesoral
FrequencyOnce daily
Preferred timingMorning

Half-life ~24-36 hours.

Safety Profile

Contraindications

  • Liver disease
  • Cardiovascular disease
  • Prostate cancer
  • Pregnancy

Common side effects

  • HPG axis suppression (dose-dependent)
  • Fatigue
  • Mild headache
  • HDL reduction

Serious risks

  • Hepatotoxicity — case reports in literature
  • Testosterone suppression
  • Lipid profile deterioration

Drug interactions

  • Avoid with other hepatotoxic compounds

Requires monitoring

  • Liver function (ALT/AST)
  • Total and free testosterone
  • Lipid panel

Pregnancy / breastfeeding

Contraindicated

Sex-Specific Notes

Male

HPG suppression documented even at 1 mg/day in healthy volunteers

Female

Limited female safety data — virilization risk

Common Misconceptions
  • Suppression is present even at low doses — not dose-free
  • Considered milder than RAD-140 but still hepatotoxic in case reports
Commonly Stacked With
MK-677 (Ibutamoren)
  • Do not stack with other SARMs
Next Steps

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