ID: ligandrol
Aliases: LGD-4033, VK5211, Anabolicum
Type: compound
Route/form: oral investigational drug in published studies
Status: investigational_or_research
Evidence level: early human
Best data tier: early human + case-report/safety
Support scope: human, non-human/mechanistic, review/regulatory
Source types: case_report, early_human, preclinical, safety_review
Linked sources: 7
Broad outcomes: Fat loss / metabolic health, Muscle growth / performance / recovery, PEDs / AAS / thermogenics, Safety / regulatory
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- androgen receptor modulator
- nonsteroidal SARM
Optimization domains
- SARM
- muscle wasting
- body composition
- bone
- doping
Research basis
- A placebo-controlled 21-day study in healthy men found dose-dependent lean-mass increases, making LGD-4033 one of the few SARMs with direct healthy-human body-composition data.
- Ovariectomized-rat muscle data provide adjacent tissue-effect support, and the entry is useful for comparing high-dose forum claims with studied exposure windows.
- Because it is common in gray-market cycles, it needs both the lean-mass signal and the liver/endocrine counter-evidence on the same page.
Limits, risks, and missing evidence
- The human study was short and surrogate-focused; it did not establish long-term performance, fertility, cardiovascular, liver, or recovery safety.
- Recent male-rat data report endurance, lipid, and hormonal downsides, and case reports link LGD-4033/off-label SARM exposure to drug-induced liver injury.
- Dose escalation and stacking with MK-677, RAD140, AAS, SERMs, or stimulants move far outside the controlled evidence.
Risk flags
- investigational
- sarm class risk
- endocrine suppression possible
- liver injury reports
- lipid risk
- doping
- short surrogate trial
Linked papers, labels, and reviews
- Safety, pharmacokinetics, and effects of LGD-4033 in healthy young men
early_human / pubmed_lgd4033_healthy_men_2013
Placebo-controlled 21-day ascending-dose study in healthy men. - LGD-4033 and MK-677 use impacts body composition and circulating biomarkers
case_report / pubmed_lgd_mk677_case_report_2022
Self-administration case report with body composition, lipid, liver enzyme, and hormone changes. - LiverTox: Selective Androgen Receptor Modulators
safety_review / ncbi_livertox_sarms_2025
NCBI LiverTox overview of SARM-associated liver injury and case literature. - Ostarine and Ligandrol Improve Muscle Tissue in an Ovariectomized Rat Model
preclinical / pubmed_ostarine_ligandrol_ovx_rat_2020
Ovariectomized-rat muscle source for ostarine and ligandrol; supports tissue effect biology but not healthy male cycle outcomes. - Ligandrol lowers endurance and negatively affects lipid and hormonal profile of male rats
preclinical / pubmed_ligandrol_endurance_lipids_hormones_rat_2025
Male-rat study reporting endurance, lipid, and hormonal downsides; useful counterweight to lean-mass-only SARM claims. - LGD-4033 and a Case of Drug-Induced Liver Injury: Exploring the Clinical Implications of Off-Label Selective Androgen Receptor Modulator Use in Healthy Adults
case_report / pubmed_ligandrol_dili_case_2024
Healthy-adult LGD-4033 DILI case report; supports liver-risk caution in off-label SARM use. - Drug-Induced Liver Injury Associated With Alpha Bolic (RAD-140) and Alpha Elite (RAD-140 and LGD-4033)
case_report / pubmed_rad_lgd_dili_case_2020
Case report involving RAD-140 and RAD-140/LGD-4033 product exposure; useful for SARM liver-risk context.