LGD-4033 (Ligandrol), product photo
SARMs

LGD-4033 (Ligandrol)

The most-used SARM in research studies on muscle mass. High androgen receptor binding affinity, low hepatotoxicity profile.

  • Ships from Germany

Order

Unit price -
  • DHL with tracking
  • Discreet packaging
At a glance

LGD-4033 (Ligandrol) by the numbers

The key figures from our lexicon. Drag the point along the curve to see how much is left after one dose, by calculation.

Full lexicon entry

How long does it stay in the body?

Share left after one dose, calculated with a half-life of ~30 hours

Half-life ~30 hours
After 60 hours: 25 %
Hour 24, next dose · 57 %Hour 30 · 50 %Hour 60 · 25 %Hour 90 · 12.5 %Hour 150 · 3.1 %

Simplified model without an absorption phase, half-life from the TPD lexicon. The lexicon gives 1 to 1.5 days, we calculate with the middle.

Class
SARM

non-steroidal

Half-life
approx. 24 to 36 hours
Use
Oral

daily

Sizes
5 to 10 mg

2 sizes in the shop

For research and educational purposes only. Values from the TPD lexicon, sources linked there.

There is no lab analysis for LGD-4033 (Ligandrol) yet. Vote for itAll lab analyses

Knowledge

Everything about LGD-4033 (Ligandrol)

Description

LGD-4033 (Ligandrol, VK5211) is a non-steroidal, oral selective androgen receptor modulator. The substance binds with high affinity to the androgen receptor (AR) and exerts agonistic effects in muscle and bone tissue, while prostatic and sebocyte activity remains comparatively low.

Per study reports LGD-4033 showed dose-dependent lean mass increase in the landmark Basaria 2013 study (JCEM) in healthy young men over 21 days. The substance was originally developed by Ligand Pharmaceuticals and later licensed to Viking Therapeutics, where it was tested as VK5211 in Phase II hip fracture rehabilitation studies.

Pharmacokinetically LGD-4033 is orally bioavailable with high bioavailability (half-life about 24-36 hours). A once-daily dose is sufficient. Compared to steroids, hepatotoxicity in available studies is moderate - moderate liver marker elevations are documented but not at the level of oral 17α-methyl steroids (Anavar, Dianabol).

Like all AR agonists, LGD-4033 suppresses the HPG axis (hypothalamus-pituitary-gonadal). Studies show drop of total testosterone and LH within days, typically recovering 4-6 weeks after discontinuation.

You can order LGD-4033 as oral tablets in one bottle with 10mg per tablet.

This information is for research and educational purposes only. No medical recommendations.

Risks & Safety

LGD-4033 sits in the mid range of the risk scale. As a high-affinity SARM the data situation is comparatively good for a SARM, but the classical class effects are documented.

Documented in studies and the literature:

  • HPG suppression: like all AR agonists, LGD-4033 suppresses the HPG axis - total testosterone and LH drop within days, with recovery typically 4-6 weeks after discontinuation.
  • HDL suppression: a lowering of HDL cholesterol is documented as a class effect of SARMs.
  • Liver markers: moderate elevations of liver enzymes are documented in the studies, though not at the level of oral 17-alpha-methyl steroids.
  • PCT requirement: because of the HPG suppression, a SERM PCT after the cycle is customary in the literature.

Monitoring via bloodwork is recommended. This classification does not replace medical advice. Risk and responsibility for any actual use lie entirely with the buyer.

Studies

Dosing

Loading dosing information …

More in the lexicon

FAQ

Frequently asked

Sources for every answer: lexicon entry

Still have a question?

Write to us, our team will help you.

Is LGD-4033 approved?

No. ChEMBL lists LGD-4033 with phase 2 as the highest phase and the registry lists one completed phase 2 study after hip fracture. WADA bans it at all times (S1.2).

What did the phase 1 study show?

76 healthy men aged 21 to 50 took placebo or one of three amounts for 21 days. Lean mass rose with the amount, fat mass did not change. Testosterone, SHBG, HDL and triglycerides fell with the amount, FSH and free testosterone only at the highest amount. After stopping the values returned. There were no drug-related serious adverse events.

What happened in older people after hip fracture?

After 12 weeks lean mass was 4.8, 7.2 and 9.1 percent above placebo depending on the dose, highest study dose 2 mg daily. At the highest dose 64 percent had at least one side effect, with placebo 36 percent. The numbers are posted in the registry, we found no journal publication.

Does LGD-4033 suppress the body's own testosterone?

Yes. Even in the short phase 1 study total testosterone fell with the amount. In rats FSH fell by about a quarter and testosterone showed a downward trend.

What is known about the liver?

In the phase 1 study the liver values AST and ALT did not change. A case report describes a 32-year-old man with severe liver injury confirmed by biopsy after taking ligandrol outside a study.

What did rat studies show about performance?

In an 8-week study submaximal endurance fell by about 30 percent with ligandrol and maximal oxygen uptake slightly. Grip strength rose, as did cholesterol and triglycerides. Training alone had favourable effects, combined with ligandrol it brought no advantage.

Comparisons

How it compares

Related

Related products