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Reference LGD-4033 (Ligandrol) 10mg FOR RESEARCH
Phase II Evidence Stage
Body Composition Primary Domain
Oral administration Routes Studied
30+ PubMed Citations
Bodycomp Peptide
Preclinical-Promising

LGD-4033 (Ligandrol)

Synthetic peptide studied in animal and cell models for lean mass accretion and tissue-selective androgen activity

Last updated: March 1, 2026

Compound Data Sheet
Peer-reviewed References
Evidence Graded
Independent Editorial
Compound
LGD-4033 (Ligandrol)
Class
Body Composition peptide
Summary
Synthetic peptide studied in animal and cell models for lean mass accretion, tissue-selective androgen activity, bone mineral density support.
Mechanism
Lean Mass Accretion and Composition Shift
Research Status
Phase II
Routes Studied
Oral administration
Evidence Level
Preclinical-promising · Clinically unproven
[ QUICK.ANSWERS ]

What Should You Know About LGD-4033 (Ligandrol)?

What is LGD-4033 (Ligandrol)?
LGD-4033 (Ligandrol) is a synthetic peptide studied in animal and cell models for lean mass accretion and tissue-selective androgen activity.
Is LGD-4033 (Ligandrol) clinically proven?
No. Human evidence remains limited and does not establish LGD-4033 (Ligandrol) as clinically proven.
What has LGD-4033 (Ligandrol) been studied for?
LGD-4033 (Ligandrol) has been studied in preclinical models of lean mass accretion, tissue-selective androgen activity, bone mineral density support. These findings have not been confirmed in large-scale human trials.
Is LGD-4033 (Ligandrol) approved?
No. LGD-4033 (Ligandrol) is not an approved drug and remains a research compound.
[ COMPOUND.PROFILE ]

What Is LGD-4033 (Ligandrol)?

LGD-4033, also known as Ligandrol or VK5211, is a non-steroidal selective androgen receptor modulator (SARM) originally developed by Ligand Pharmaceuticals and subsequently licensed to Viking Therapeutics for clinical development. With the molecular formula C14H12F6N2O and a molecular weight of 338.25 g/mol, LGD-4033 is a small synthetic molecule that binds to androgen receptors with high affinity and selectivity. It is classified as a SARM, not a peptide, anabolic steroid, or prohormone,...

[ EVIDENCE.SUMMARY ]

Evidence Summary

Preclinical-promising · Clinically unproven

LGD-4033 (Ligandrol) is a research compound with promising biological signals but limited human validation. Most claims exceed current clinical evidence.

Evidence Breakdown

Domain Evidence Level
Lean Mass Accretion Limited
Tissue-Selective Androgen Activity Limited
Bone Mineral Density Support Limited
Oral Bioavailability and Convenience Limited
Human clinical evidence Limited
Safety data Insufficient

Editorial Position

LGD-4033 (Ligandrol) is best understood as a compound with emerging clinical evidence that has not yet reached definitive conclusions. Many online claims exceed the strength of available human evidence, and safety data remains incomplete. Any consideration of this compound should involve careful evaluation of individual context and medical guidance.

Regulatory Status Snapshot

  • Not approved as a therapeutic drug by major regulators
  • Safety profile not established in large human populations

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[ STUDIED.FOR ]

What Has LGD-4033 (Ligandrol) Been Studied For?

Research areas where LGD-4033 (Ligandrol) has been investigated in published studies

  • Lean Mass Accretion LGD-4033 (Ligandrol) has been studied in animal models of lean mass accretion. These findings have not been confirmed in controlled human trials.
  • Tissue-Selective Androgen Activity LGD-4033 (Ligandrol) has been studied in animal models of tissue-selective androgen activity. These findings have not been confirmed in controlled human trials.
  • Bone Mineral Density Support LGD-4033 (Ligandrol) has been studied in animal models of bone mineral density support. These findings have not been confirmed in controlled human trials.
  • Oral Bioavailability and Convenience LGD-4033 (Ligandrol) has been studied in animal models of oral bioavailability and convenience. These findings have not been confirmed in controlled human trials.
[ MECHANISM ]

How Does LGD-4033 (Ligandrol) Work?

These mechanisms have been observed in preclinical models. They are plausible but have not been linked to proven clinical outcomes in humans.

  1. 01 Selective Androgen Receptor Binding
  2. 02 Tissue-Specific Co-Regulator Recruitment
  3. 03 Downstream biological effect
  4. 04 Osteoblast Stimulation in Bone
NEXT STEP

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A specialist can review the evidence, evaluate your medical context, and help you make an informed decision about LGD-4033 (Ligandrol).

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[ COMMUNITY.FEEDBACK ]

Community Reports (Anecdotal)

Experiences shared here are self-reported and do not represent clinical evidence.

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[ ADMINISTRATION ]

How Is LGD-4033 (Ligandrol) Administered?

LGD-4033 (Ligandrol) is available via Oral administration. Appropriate use and protocol should be determined by a qualified specialist.

[ REFERENCE.DATA ]

What Are the Specifications of LGD-4033 (Ligandrol)?

Format Lyophilized Powder
Amount 10mg per vial
Purity >99%
Purity Method HPLC (High-Performance Liquid Chromatography)
Composition LGD-4033 (Ligandrol/VK5211), non-steroidal SARM
Molecular Weight 338.25 g/mol
Storage Store at room temperature (15-25°C) in a dry, light-protected environment.
Appearance White crystalline powder
[ EXPLORE ]

What Conditions Has LGD-4033 (Ligandrol) Been Linked To?

Have Questions About LGD-4033 (Ligandrol)?

Yes. LGD-4033 is classified as a prohibited substance by the World Anti-Doping Agency (WADA) under the category S1.2 (Other Anabolic Agents). It is also banned by most professional and amateur athletic organizations.

Published studies on LGD-4033 (Ligandrol) can be found on PubMed and other peer-reviewed databases. Our references section below lists key citations.

LGD-4033 (Ligandrol) is available as a research compound in Thailand. Consult a qualified specialist to discuss whether it is appropriate for your needs.

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EDITORIAL REVIEW

Reviewed by the Peptide Science Thailand Editorial Team.

Last reviewed: March 1, 2026

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The information provided on this website, including compound profiles, mechanism of action explanations, research summaries, dosage information, and educational content, is for informational and educational purposes only. This information does not constitute medical advice, diagnosis, or treatment recommendations. No content on this website should be interpreted as a substitute for professional medical advice, diagnosis, or treatment.

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All peptide compounds discussed on this website should only be used under the supervision of a qualified specialist. A healthcare provider should evaluate individual health status, medical history, current medications, and specific health objectives before any peptide use. Self-administration of research peptides without medical supervision is strongly discouraged and may pose significant health risks.

Individual Variation

Individual responses to peptide compounds vary significantly based on genetics, age, body composition, existing health conditions, concurrent medications, and other biological factors. Dosage information provided on this website represents general research ranges and should not be used for self-dosing. A qualified specialist should determine the appropriate compound, dosage, administration route, cycle duration, and monitoring protocol based on individual health assessment.

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Regulatory Status

Many peptides discussed here have not been evaluated or approved by the FDA for therapeutic use unless specifically noted (e.g., Tesamorelin, PT-141). The regulatory status of peptide compounds varies by jurisdiction. Some compounds discussed on this website are approved medications in other countries (e.g., Semax and Selank in Russia). This content is for informational and educational purposes only. Users are responsible for understanding and complying with all applicable laws and regulations in their jurisdiction.