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title: "LGD-4033 (Ligandrol): Dosing &amp; Vendor Prices"
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# LGD-4033 (Ligandrol)

Performance Phase 2 

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Also known as: Ligandrol, LGD4033, LGD 4033, VK5211, VK-5211, Anabolicum 

LGD-4033, usually sold as ligandrol, is a nonsteroidal selective androgen receptor modulator that Viking Therapeutics took into clinical development under the code VK5211 (NCT02578095). The stated development goal was an oral drug that produces the muscle and bone effects of testosterone with less action on prostate and skin, aimed at conditions such as recovery after hip fracture and other causes of muscle loss.

Half-Life:  Long elimination half-life in humans with dose-proportional accumulation over 21 days of daily dosing in healthy young men; the report describes the profile without giving a single value in its summary (PMID: 22459616) Route:  Oral MW:  338.25 g/mol CAS:  1165910-22-4 

Last reviewed: Sep 7, 2026 

[

Performance

Category



](/wiki#cat-performance)

Phase 2

Research Stage

OverviewChemical InfoDosing & ProtocolsInteractionsResearchCompare Prices1 Related

## Overview

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### At A Glance

Mechanism 

LGD-4033 binds the androgen receptor with high affinity and selectivity and acts as a nonsteroidal agonist, driving transcription of androgen-responsive genes in skeletal muscle and bone while sparing prostate to a greater degree than testosterone (PMID: 22459616). Because the re… 

Half-Life 

Long elimination half-life in humans with dose-proportional accumulation over 21 days of daily dosing in healthy young men; the report describes the profile without giving a single value in its summary (PMID: 22459616)

Routes 

Oral 

Potential Benefits 

Increased lean body mass without a change in fat mass over 21 days in healthy young men in a placebo-controlled phase 1 study (PMID: 22459616) Improved muscle tissue in ovariectomized rats (PMID: 33042018) Improved trabecular bone structural properties at the highest dose tested in ovariectomized rats (PMID: 37407738) 

### Overview

LGD-4033, usually sold as ligandrol, is a nonsteroidal selective androgen receptor modulator that Viking Therapeutics took into clinical development under the code VK5211 (NCT02578095). The stated development goal was an oral drug that produces the muscle and bone effects of testosterone with less action on prostate and skin, aimed at conditions such as recovery after hip fracture and other causes of muscle loss. It has not been approved by any regulator, and clinical development has not progressed past phase 2. Mechanistically it binds the androgen receptor with high affinity and selectivity and acts as an agonist in muscle and bone. The consequences of that binding are visible in the human phase 1 data: over three weeks of daily dosing in healthy young men, total testosterone, sex hormone binding globulin, HDL cholesterol and triglycerides all fell in a dose-dependent way, follicle-stimulating hormone and free testosterone fell at the top dose, and lean body mass rose without a change in fat mass (PMID: 22459616). Hormone levels and lipids returned to baseline after the drug was stopped in that 21-day study, which is a short exposure compared with how the compound is used outside research. Animal work supports an anabolic signal but is mixed on whether that translates to performance. In ovariectomized rats, ligandrol improved muscle tissue (PMID: 33042018) and improved trabecular bone structure at the highest dose tested in ovariectomized rats (PMID: 37407738). In male rats, however, ligandrol lowered endurance and worsened lipid and hormonal profiles (PMID: 40087185). Human safety reports are the strongest reason for caution. Published case reports describe severe cholestatic liver injury confirmed on biopsy after ligandrol use, including a 32-year-old man with cholestatic hepatitis and fibrosis (PMID: 32637435), a 37-year-old man with bilirubin about thirty times the upper limit of normal and ductopenia on biopsy (PMID: 36257328), a further case in an otherwise healthy adult (PMID: 39421081) and cases involving ligandrol together with post-cycle drugs (PMID: 34141767). A retrospective Australian series of drug-induced liver injury from anabolic steroids, SARMs and bodybuilding supplements collected 23 cases, most of whom were admitted to hospital, with a median 175 days to normal liver biochemistry and one liver transplant (PMID: 38372012). A self-reported case of ligandrol taken with the growth hormone secretagogue MK-677 recorded alanine aminotransferase up about 205 percent, HDL cholesterol down about 36 percent and total testosterone down about 62 percent (PMID: 36303408). In sport, LGD-4033 is prohibited at all times under the World Anti-Doping Agency class S1.2 and has been found in athlete urine samples (PMID: 27168428). Its human urinary metabolites are well characterized for testing purposes (PMID: 30255601). FDA has issued warning letters to firms selling it as an unapproved new drug (FDA warning letter to Titan SARMs LLC, 12 December 2025). What is sold as ligandrol is often mislabeled: in an analysis of 44 SARM-marketed products, only about half contained any SARM and the label amount matched the assay in 41 percent (PMID: 29183075).

### Potential Research Fields

Muscle wasting and sarcopenia Bone and fracture recovery Sports drug testing Hepatotoxicity surveillance 

## Chemical Information

IUPAC Name

Not yet available 

CAS Number

1165910-22-4

Molecular Formula

C14H12F6N2O

Molecular Mass

338.25 g/mol

![LGD-4033 (Ligandrol) molecular structure](https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/cid/44137686/PNG)

[View on PubChem](https://pubchem.ncbi.nlm.nih.gov/compound/44137686)

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## Interactions

### Contraindications

Mechanism-based: contraindicated in pregnancy because androgen receptor agonists can virilize a female fetus, and in men with known or suspected prostate cancer. Existing liver disease or raised transaminases is a case-report-based reason to avoid it (PMID: 32637435, PMID: 36257328). Because it suppresses endogenous testosterone and gonadotropins (PMID: 22459616), it works against men being treated for infertility. Prohibited for athletes in tested sport at all times (PMID: 28137616).

Research Disclaimer

This interaction data is compiled from published research and community reports. It may not be exhaustive. Always consult a healthcare professional before combining compounds.

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Current low

$84.99

as of Sep 7, 2026

7-day low

$84.99

30-day low

$84.99

30-day change

— 

baseline building

Tracking since Sep 7, 2026 · 1 data point

### Vendors Selling LGD-4033 (Ligandrol)

[

![Disguised Alpha logo](https://disguisedalpha.com/wp-content/themes/assets/logos/disguised-logo-2x.png)

#### Disguised Alpha

1 listing · from $84.99 





](/vendor/disguised-alpha)

How we score these vendors

Every supplier above is graded 0–100 on COA verification, payment transparency, shipping, reviews, and active listings. Methodology published, no pay-to-rank.

[View Scorecard](/vendors/scorecard)

### Related Compounds

[View All](/wiki)

[

### ITPP

Performance Preclinical 

ITPP (myo-inositol trispyrophosphate, sometimes written myo-inositol tripyrophosphate or OXY111A in NormOxys trial documents) is a small-molecule allosteric effector of hemoglobin designed to increase the amount of oxygen red blood cells release to tissues.

Research compound — IV infusion in studies, no established oral doses 

36 studies View Profile 

](/compound/itpp)[

### Ostarine (Enobosarm, MK-2866)

Performance Phase 3 

Ostarine is the market name for enobosarm, a nonsteroidal selective androgen receptor modulator first developed by GTx Inc under the codes GTx-024, MK-2866 and S-22.

t½ Not established from a retrieved human report; in rats the mean elimination half-life of radiolabeled GTx-024 was 0.6 h in males and 16.4 h in females (PMID: 24074268). Human plasma pharmacokinetics were characterized in phase 1 drug-interaction studies (PMID: 27105861) 

Preclinical View Profile 

](/compound/ostarine)[

### PEG-MGF

Performance Preclinical 

PEG-MGF (Pegylated Mechano Growth Factor) is a synthetic, PEGylated form of Mechano Growth Factor (MGF) — an alternatively spliced variant of IGF-1 produced locally in muscle and other tissues in response to mechanical loading or damage.

t½ Native MGF: very short (minutes) due to rapid proteolysis. PEG-MGF: PEGylation is intended to extend this substantially (community estimates up to roughly 1 day), but there are no published human pharmacokinetic data to confirm a specific value.  200 

Preclinical View Profile 

](/compound/peg-mgf)[

### RAD-140 (Testolone)

Performance Phase 1 

RAD-140, sold as testolone and given the international nonproprietary name vosilasarm, is a nonsteroidal selective androgen receptor modulator developed at Radius Health, whose scientists reported the first-in-human trial (PMID: 34565686), and first described in the medicinal chemistry literature as a compound with an oxadiazole core designed for oral androgen receptor activity with tissue selectivity (PMID: 24900290).

t½ Terminal half-life 44.7 hours in humans, measured in a first-in-human phase 1 study in postmenopausal women with metastatic breast cancer (PMID: 34565686) 

Preclinical View Profile 

](/compound/rad-140)[

### SLU-PP-332

Performance Preclinical 

SLU-PP-332 is the first-generation synthetic pan-agonist of the estrogen-related receptors (ERRα, ERRβ, ERRγ) developed by the laboratory of Thomas Burris at Saint Louis University and reported in a landmark 2023 publication that established ERR pan-agonism as a pharmacologically tractable exercise-mimetic drug mechanism.

Research compound — no established human doses. Animal studies: 10-50 mg/kg 

8 studies View Profile 

](/compound/slu-pp-332)[

### YK-11

Performance Preclinical 

YK-11 is a synthetic steroid, not a nonsteroidal SARM, despite being sold alongside them.

t½ Not established. In a human elimination study using deuterium-labeled YK-11, no intact parent compound was seen in urine; unconjugated metabolites disappeared within 24 hours and glucuronidated and sulfated metabolites remained traceable beyond 48 hours (PMID: 30379415) 

Preclinical View Profile 

](/compound/yk-11)

[

View Full Dosage Guide →

Protocols, calculator & safety for LGD-4033 (Ligandrol)



](/guides/dosage/lgd-4033)

### Best Price

![Disguised Alpha logo](https://disguisedalpha.com/wp-content/themes/assets/logos/disguised-logo-2x.png)

Disguised Alpha

$84.99

[Buy Now](https://disguisedalpha.com/product/lgd4033/?coupon=reddit)

1 vendors · 1 listings

### Research Score

30 

0 PubMed studies

### Quality Indicators

Data Completeness

63% 

Description 

Mechanism of Action 

Chemical Data 

Dosing Protocols 

Safety Profile 

PubMed Studies 

Interactions 

Vendor Listings 

### Quick Facts

Half-Life

Long elimination half-life in humans with dose-proportional accumulation over 21 days of daily dosing in healthy young men; the report describes the profile without giving a single value in its summary (PMID: 22459616)

Molecular Weight

338.25 g/mol

Administration

Oral

CAS Number

1165910-22-4

Trial Phase

Phase 2

0

[Full Dosage Guide](/guides/dosage/lgd-4033)[Calculate Your Dose](/tools/reconstitution)

Research Disclaimer

This information is for educational and research purposes only. Not intended as medical advice. Consult a healthcare professional before use.

## Frequently Asked Questions

What is LGD-4033 (Ligandrol) used for in research?

LGD-4033, usually sold as ligandrol, is a nonsteroidal selective androgen receptor modulator that Viking Therapeutics took into clinical development under the code VK5211 (NCT02578095). The stated development goal was an oral drug that produces the muscle and bone effects of testosterone with less action on prostate and skin, aimed at conditions such as recovery after hip fracture and other causes of muscle loss. It has not been approved by any regulator, and clinical development has not progressed past phase 2.

Mechanistically it binds the androgen receptor with high affinity and selectivity and acts as an agonist in muscle and bone. The consequences of that binding are visible in the human phase 1 data: over three weeks of daily dosing in healthy young men, total testosterone, sex hormone binding globulin, HDL cholesterol and triglycerides all fell in a dose-dependent way, follicle-stimulating hormone and free testosterone fell at the top dose, and lean body mass rose without a change in fat mass (PMID: 22459616). Hormone levels and lipids returned to baseline after the drug was stopped in that 21-day study, which is a short exposure compared with how the compound is used outside research.

Animal work supports an anabolic signal but is mixed on whether that translates to performance. In ovariectomized rats, ligandrol improved muscle tissue (PMID: 33042018) and improved trabecular bone structure at the highest dose tested in ovariectomized rats (PMID: 37407738). In male rats, however, ligandrol lowered endurance and worsened lipid and hormonal profiles (PMID: 40087185).

Human safety reports are the strongest reason for caution. Published case reports describe severe cholestatic liver injury confirmed on biopsy after ligandrol use, including a 32-year-old man with cholestatic hepatitis and fibrosis (PMID: 32637435), a 37-year-old man with bilirubin about thirty times the upper limit of normal and ductopenia on biopsy (PMID: 36257328), a further case in an otherwise healthy adult (PMID: 39421081) and cases involving ligandrol together with post-cycle drugs (PMID: 34141767). A retrospective Australian series of drug-induced liver injury from anabolic steroids, SARMs and bodybuilding supplements collected 23 cases, most of whom were admitted to hospital, with a median 175 days to normal liver biochemistry and one liver transplant (PMID: 38372012). A self-reported case of ligandrol taken with the growth hormone secretagogue MK-677 recorded alanine aminotransferase up about 205 percent, HDL cholesterol down about 36 percent and total testosterone down about 62 percent (PMID: 36303408).

In sport, LGD-4033 is prohibited at all times under the World Anti-Doping Agency class S1.2 and has been found in athlete urine samples (PMID: 27168428). Its human urinary metabolites are well characterized for testing purposes (PMID: 30255601). FDA has issued warning letters to firms selling it as an unapproved new drug (FDA warning letter to Titan SARMs LLC, 12 December 2025). What is sold as ligandrol is often mislabeled: in an analysis of 44 SARM-marketed products, only about half contained any SARM and the label amount matched the assay in 41 percent (PMID: 29183075).

What forms does LGD-4033 (Ligandrol) come in?

LGD-4033 (Ligandrol) is available in liquid form.

How much does LGD-4033 (Ligandrol) cost?

Prices start at $84.99 across 1 verified vendor.

How do I compare LGD-4033 (Ligandrol) vendors?

Compare prices, payment methods, shipping, and COA scores across 1 vendor.

## Research Tools

[

### Peptide Calculator

Reconstitution & syringe units



](/tools/reconstitution)[

### Reconstitution Guide

How to mix, step by step



](/guides/how-to-reconstitute-peptides)[

### Nasal Spray Calc

mL per actuation



](/tools/intranasal)[

### Half-Life Visualizer

Decay curves



](/tools/halflife)

## Related Compounds

[View All](/wiki)

[

### ITPP

Performance Preclinical 

ITPP (myo-inositol trispyrophosphate, sometimes written myo-inositol tripyrophosphate or OXY111A in NormOxys trial documents) is a small-molecule allosteric effector of hemoglobin designed to increase the amount of oxygen red blood cells release to tissues.

Research compound — IV infusion in studies, no established oral doses 

36 studies View Profile 

](/compound/itpp)[

### Ostarine (Enobosarm, MK-2866)

Performance Phase 3 

Ostarine is the market name for enobosarm, a nonsteroidal selective androgen receptor modulator first developed by GTx Inc under the codes GTx-024, MK-2866 and S-22.

t½ Not established from a retrieved human report; in rats the mean elimination half-life of radiolabeled GTx-024 was 0.6 h in males and 16.4 h in females (PMID: 24074268). Human plasma pharmacokinetics were characterized in phase 1 drug-interaction studies (PMID: 27105861) 

Preclinical View Profile 

](/compound/ostarine)[

### PEG-MGF

Performance Preclinical 

PEG-MGF (Pegylated Mechano Growth Factor) is a synthetic, PEGylated form of Mechano Growth Factor (MGF) — an alternatively spliced variant of IGF-1 produced locally in muscle and other tissues in response to mechanical loading or damage.

t½ Native MGF: very short (minutes) due to rapid proteolysis. PEG-MGF: PEGylation is intended to extend this substantially (community estimates up to roughly 1 day), but there are no published human pharmacokinetic data to confirm a specific value.  200 

Preclinical View Profile 

](/compound/peg-mgf)[

### RAD-140 (Testolone)

Performance Phase 1 

RAD-140, sold as testolone and given the international nonproprietary name vosilasarm, is a nonsteroidal selective androgen receptor modulator developed at Radius Health, whose scientists reported the first-in-human trial (PMID: 34565686), and first described in the medicinal chemistry literature as a compound with an oxadiazole core designed for oral androgen receptor activity with tissue selectivity (PMID: 24900290).

t½ Terminal half-life 44.7 hours in humans, measured in a first-in-human phase 1 study in postmenopausal women with metastatic breast cancer (PMID: 34565686) 

Preclinical View Profile 

](/compound/rad-140)[

### SLU-PP-332

Performance Preclinical 

SLU-PP-332 is the first-generation synthetic pan-agonist of the estrogen-related receptors (ERRα, ERRβ, ERRγ) developed by the laboratory of Thomas Burris at Saint Louis University and reported in a landmark 2023 publication that established ERR pan-agonism as a pharmacologically tractable exercise-mimetic drug mechanism.

Research compound — no established human doses. Animal studies: 10-50 mg/kg 

8 studies View Profile 

](/compound/slu-pp-332)[

### YK-11

Performance Preclinical 

YK-11 is a synthetic steroid, not a nonsteroidal SARM, despite being sold alongside them.

t½ Not established. In a human elimination study using deuterium-labeled YK-11, no intact parent compound was seen in urine; unconjugated metabolites disappeared within 24 hours and glucuronidated and sulfated metabolites remained traceable beyond 48 hours (PMID: 30379415) 

Preclinical View Profile 

](/compound/yk-11)

Free 2026 Peptide Cheat Sheet — 50 pages, PDF

Reconstitution math, concentration charts, half-lives, and vendor trust tiers. The reference we wish we had on day one.

[Download Free](/guides/peptide-cheat-sheet-download?utm_source=compound-lgd-4033)

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