LGD 4033 by Dragon Pharma

Dragon Pharma Original Formula

LGD-4033 (Ligandrol)

VK521115 mg/tab
Class Non-Steroidal SARM
Half-Life ~24–36 hours
Anabolic Potency Strongest Available SARM
Suppression Significant (HPG)
Pack 100 tabs
Form Oral Tablet
Availability: In Stock
$95.00
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LGD-4033 (Ligandrol) — Strongest SARM by Dragon Pharma

LGD-4033 (Ligandrol, VK5211) is Dragon Pharma's formulation of the most anabolically potent widely available SARM at 15mg per tablet — developed by Ligand Pharmaceuticals and subsequently licenced to Viking Therapeutics. LGD-4033 has completed Phase I human clinical trials, providing genuine human pharmacokinetic and lean mass data at doses far below typical performance use. It produces significantly greater lean mass gains than Ostarine at equivalent doses, with correspondingly greater HPG axis suppression — the most important trade-off to understand when positioning LGD-4033 within the SARM hierarchy.

Also searched as: LGD-4033 Ligandrol, LGD 4033 15mg, Ligandrol Dragon Pharma, VK5211, Ligandrol SARM tabs.

The Phase I Clinical Trial Data

LGD-4033 has more rigorous human clinical evidence than most SARMs — but the data needs careful interpretation for performance use:

  • Basaria et al. (2010, Journal of Gerontology) conducted a Phase I ascending-dose study in 76 healthy young men — randomised to placebo or LGD-4033 at 0.1mg, 0.3mg or 1.0mg/day for 21 days. Results: dose-dependent increases in lean body mass (0.3kg at 0.1mg, 0.6kg at 1.0mg over 21 days); significant dose-dependent decreases in total testosterone, SHBG, LH and FSH; and fat mass reductions at higher doses
  • The key clinical finding: at just 1.0mg/day for 21 days, LGD-4033 produced meaningful lean mass gains and significant HPG suppression. Performance users typically use 5-15mg/day — doses 5-15× higher than the clinical trial maximum, for cycle lengths 4-6× longer
  • No prostate-specific effects (PSA) were observed at clinical doses — consistent with SARM tissue selectivity. No significant liver enzyme elevation at clinical doses — though performance doses and durations exceed the clinical trial parameters
  • Recovery after the 21-day clinical trial: testosterone, SHBG, LH and FSH returned to baseline within 5 weeks of cessation at 1mg/day dose — suggesting HPG recovery at clinical doses, though performance doses produce more substantial suppression with potentially longer recovery

LGD-4033 vs Ostarine — The SARM Potency Comparison

Understanding LGD-4033 requires understanding how it differs from Ostarine (MK-2866), the most commonly referenced SARM:

Parameter LGD-4033 (Ligandrol) Ostarine (MK-2866)
Anabolic potency High — significantly stronger Mild-moderate
Lean mass gains 3–5 kg in 8-week cycle typical 1–3 kg in 8-week cycle typical
Suppression degree Significant — testosterone suppression substantial Mild — 20-40% LH/FSH reduction
Clinical human data Phase I data at 0.1-1.0mg/day Phase III data (3mg/day, cancer cachexia)
PCT required Yes — standard PCT advisable for all cycles Advisable for 8+ week cycles at 25mg
Bone density effects Yes — high AR affinity in bone tissue Some — documented in clinical data
Best use case Mass building; strength; recomposition Lean mass preservation; injury support; first SARM

The Suppression Reality at Performance Doses

LGD-4033's suppression at performance doses (5-15mg/day) is substantially greater than at clinical doses (0.1-1.0mg/day) and requires honest discussion:

  • At 5mg/day for 8 weeks, user-reported testosterone suppression of 50-70% from baseline is commonly documented — significantly greater than Ostarine's typical 20-40%
  • At 10-15mg/day, near-complete LH and FSH suppression is reported by many users — with testosterone falling to very low levels, requiring the same attentiveness to PCT as after an injectable AAS cycle
  • The 24-36 hour half-life means once-daily dosing produces stable blood levels, but also means the compound is continuously suppressive throughout the cycle with no "recovery days"
  • PCT timing: LGD-4033 has a 24-36 hour half-life — PCT can begin 24-48 hours after the last tablet, similar to Ostarine. A standard 4-6 week PCT with Clomid or Nolvadex is advisable after cycles of 8+ weeks at standard performance doses

LGD-4033 in the Full SARM Comparison

SARM Anabolic Potency Suppression Clinical Data Best Application
LGD-4033 Highest available Significant Phase I human trial Mass; strength; recomposition
MK-2866 (Ostarine) Mild-Moderate Mild Phase III human trial Lean mass; injury; first SARM
YK-11 Very high Significant Preclinical only Myostatin inhibition; strength
S23 High High Preclinical only Cutting; hardness

Effects and Benefits

  • Highest anabolic potency among widely available SARMs — 3-5kg lean mass gains in a typical 8-week performance cycle
  • Significant strength increases — AR activation in muscle tissue drives protein synthesis and neuromuscular efficiency
  • Bone density support — LGD-4033 has demonstrated bone mineral density effects in clinical models, making it relevant for injury prevention and bone health
  • No aromatisation — no direct estrogenic side effects from LGD-4033 itself
  • Oral — no injection required

Dosage and Administration

Experience Level Daily Dose Cycle Length PCT
First LGD cycle 5 mg/day (⅓ tablet) 6–8 weeks 4-week Clomid/Nolvadex
Standard performance 10 mg/day (⅔ tablet) 8 weeks 4-6 week PCT
Advanced 15 mg/day (1 tablet) 8 weeks 6-week PCT advisable

At 15mg per tablet, the standard 10mg performance dose requires splitting the tablet (⅔). The 24-36 hour half-life supports once-daily dosing — morning or evening both work. At the full 15mg tablet dose, suppression is pronounced and PCT is as important as after an injectable AAS cycle. Never stack with other suppressive compounds without understanding the additive suppression.

PCT for LGD-4033

  • Clomid — 50mg/day for 2 weeks, then 25mg/day for 2 weeks; start 24-48 hours after last LGD tablet
  • Nolvadex — 40mg/day for 2 weeks, then 20mg/day for 2 weeks; same timing
  • At 10-15mg/day cycles, a 6-week PCT may be warranted given the more significant suppression compared to Ostarine

LGD-4033 in a Stack

  • MK-677 — oral GH secretagogue adds GH/IGF-1 elevation to LGD-4033's AR-driven anabolic effects; a fully injectable-free mass and recovery stack
  • GW-501516 (Cardarine) — PPARδ endurance support alongside LGD-4033's mass building; addresses the cardiovascular and endurance demands of high-volume mass training

"LGD-4033 is the strongest anabolic SARM available — Phase I human trial data confirms meaningful lean mass gains at just 1mg/day, with dose-dependent suppression that at performance doses (5-15mg/day) requires the same PCT attentiveness as an injectable AAS cycle."

Storage and Handling

Store LGD-4033 at room temperature, away from direct sunlight and moisture. Keep in original packaging until use.

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Basaria et al. (2010) conducted a Phase I dose-ascending study in 76 healthy young men randomised to placebo or LGD-4033 at 0.1mg, 0.3mg or 1.0mg/day for 21 days. Results showed dose-dependent increases in lean body mass (up to 0.6kg at 1.0mg over 21 days), significant dose-dependent decreases in total testosterone, SHBG, LH and FSH, no significant PSA changes, and no liver enzyme elevation at clinical doses. Performance users typically use 5-15mg/day — 5-15× higher than the clinical trial maximum — for 6-8× longer duration, so clinical safety data does not directly extrapolate to performance use.

LGD-4033 produces significantly greater lean mass gains than Ostarine at any comparable dose — typically 3-5kg in an 8-week performance cycle at 10mg/day versus 1-3kg for Ostarine at 25mg/day. This superior anabolic potency comes with correspondingly greater HPG axis suppression: Ostarine at 25mg/day typically suppresses LH/FSH by 20-40%; LGD-4033 at 5-15mg/day produces 50-70% or greater testosterone suppression in most users, requiring the same PCT attentiveness as an injectable AAS cycle.

Yes — always, for any cycle of meaningful dose and duration. At 5mg/day for 6 weeks, some users recover without formal PCT, but at 10-15mg/day for 8 weeks, suppression is substantial enough to warrant a full 4-6 week PCT with Clomid or Nolvadex. PCT begins 24-48 hours after the last LGD-4033 tablet — the 24-36 hour half-life means blood levels clear relatively quickly, unlike long-ester injectable AAS. The depth of suppression at performance doses means PCT should not be skipped even though LGD-4033 is "not a steroid."

Yes — LGD-4033 can be used as an addition to a testosterone base, though the combined suppression means PCT is essential. The most practical SARM context for injectable testosterone stacking is to add LGD-4033 as an oral mass compound to a testosterone base, similar to adding Dianabol or Winstrol. The non-aromatising property of LGD-4033 means only the testosterone component needs AI management.

VK5211 is simply the development name given to LGD-4033 by Viking Therapeutics after they licenced the compound from Ligand Pharmaceuticals for further clinical development — specifically for hip fracture recovery (where LGD-4033's combined muscle and bone-building effects are relevant). The compound is identical: LGD-4033 = Ligandrol = VK5211. The VK5211 name appears in some later clinical development literature but refers to the same molecule.

Yes — LGD-4033 and its metabolites are detectable in urine for several weeks after the last dose using standard sports anti-doping panels. WADA includes SARMs on the prohibited list. Competitive athletes in tested sport should not use LGD-4033. Detection windows extend beyond the visible half-life due to metabolite persistence in urine.

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