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GW501516 Cardarine 20mg - Dragon Pharma

Dragon Pharma

GW501516 Cardarine 20mg - Dragon Pharma

Oral · 20 mg/tab · 100 tabs

In stock · ships within 24h Out of stock Ships from International · U.S Domestic
CompoundCardarine (GW501516)
ClassPPAR-delta agonist
Half-lifeNot established
DetectionUp to 40 days
Liver toxicityNot established
Water retentionNone
Twenty milligram tablets of a PPAR-delta agonist, 100 to a pack. Nothing here touches an androgen receptor, so there is no aromatisation and no suppression of the hormonal axis, which is why the half-life and liver rows read Not established: the cited sources simply do not supply those numbers, and they are not invented here for appearance. Detection is the one well documented figure, and it runs the other way from anabolic steroids: sulfone metabolites in urine are reported up to 40 days after a single dose while the parent drug clears within about 5 days. Development was abandoned in 2007 after cancer appeared rapidly in several organs in mice and rats.
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GW501516 Cardarine 20mg - Dragon Pharma
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All products are manufactured under strict quality standards and independently tested before release. By purchasing, the buyer agrees to use these products in compliance with all applicable laws.

Product Overview

GW501516 Cardarine by Dragon Pharma sits at the centre of this page. The pack is 100 tablets at 20 mg, and the compound is a PPAR-delta agonist, a metabolic modulator that became famous under the nickname cardio in a tablet. It is not a SARM and not a steroid. Nothing in this molecule touches the androgen receptor, nothing aromatises, and the hormonal axis that steroids suppress is left alone.

That clean hormone profile is only half the story, and the other half is the reason this page reads differently from the rest of the range. Development of GW501516 was abandoned in 2007 after cancer appeared rapidly across multiple organs in mice and rats, and WADA has issued separate warnings that the substance is not safe. The dosing figures below are practice, not study results, and they should be read next to that signal.

Cardarine, also catalogued as GW1516, GSK-516 and endurobol, activates the PPAR-delta receptor, one of the nuclear receptors that govern how muscle fibres handle fat as fuel. It surfaced in endurance research because treated animals ran substantially further before exhaustion, and that single result created a black market almost overnight. What the research programme never produced was a human safety dossier, because the carcinogenicity findings in two rodent species ended it.

The pack on this card holds 100 tablets, each carrying 20 mg, from Dragon Pharma. Two short-card rows on this page read Not established, and that is deliberate: the cited sources do not provide a half-life for the compound and do not assign a liver toxicity rating to a PPAR agonist. Those cells are empty because the data is missing, not because nobody filled them in. The one well documented number on the card is detection, and it runs the opposite way from anabolic steroids: sulfone metabolites in urine are reported for up to 40 days after a single dose, while the parent drug itself clears within roughly 5 days.

Mechanism of Action

PPAR-delta is a transcription factor that shifts skeletal muscle toward burning fat and away from storing it. When the receptor is activated, the muscle increases its capacity for fatty acid oxidation and the profile of muscle fibres drifts toward the oxidative end, which is the mechanistic reason the animals in the endurance studies kept going. Glucose handling also improves in the same pathway, which is why metabolic markers and lipid profile come up in the literature.

Two consequences follow from that mechanism. First, none of it involves hormones, so there is no aromatisation, no water retention and no shutdown of testosterone production; a SERM recovery protocol has nothing to recover. Second, the same receptor pathway is the site of the cancer signal. In the rodent studies that ended the programme, animals given about 3 mg per kilogram per day developed tumours in several organs within a short period, and there is no human dataset that tells you where the safe boundary sits. Receptor-level reasoning cannot make that risk disappear, and this page will not pretend otherwise.

Dosage Protocol

The tablet is taken once a day. The figures below are the ones that circulate, and they are tagged as practice because no human protocol survived the closure of the development programme.

Starting dose 10 mg a day, once daily
Common range 10-20 mg a day
Upper range 20 mg a day; anything above sits outside the available data
Block length 8 weeks for a first block, up to 12 in practice
Administration Oral tablet, 20 mg strength, supply of 100 per pack
Female use Sources describe no female protocol for cardarine

Because the hormonal axis is untouched, the usual recovery logic does not apply and cycling off is about limiting exposure rather than restarting anything. That is the reason a shorter block is the sensible default here: the unknown in this molecule is dose and duration dependent, and every extra week adds exposure without adding evidence.

Suggested Protocols

Cardarine is combined in practice with compounds that work on unrelated pathways, which keeps the logic simple even though none of the combinations is supported by trial data.

Endurance and lean mass research
GW501516 Cardarine - 10-20 mg a day + Ostarine (MK 2866) at 25 mg daily
Metabolic and androgen-receptor effects sit on separate pathways; the SARM side still needs its own recovery thinking
Conditioning with a GH secretagogue
GW501516 Cardarine - 10-20 mg a day + Ibutamoren (MK 677), 25 mg daily
Appetite from the secretagogue works against the fat loss goal; monitor glucose and weight together
Recomposition arrangement
GW501516 Cardarine - 10-20 mg a day + LGD 4033, 15 mg daily + YK 11 - 10 mg a day
Two suppressive SARMs plus a metabolic agent; the androgen load is what makes monitoring necessary

What to Expect

Reports on this compound cluster around endurance and conditioning rather than size, and the timelines come from non-medical use.

Endurance: animal work showed large increases in running capacity, which is what created the demand.
Lipid profile: improvement is discussed as a metabolic effect of receptor activation.
Body composition: changes in fat and lean tissue are discussed, but human data is limited.
Hormones: nothing here suppresses the axis or raises estrogen, so cycles need no hormonal rescue.
Onset: users describe noticing the effect within 2-4 weeks of daily dosing.
Ceiling: development stopped in 2007, so there is no long-term human experience to draw on.

The practical expectation for a person reading this card is modest performance change paired with a genuine and unresolved safety signal. Anyone unwilling to accept the second should not be considering the first.

Side Effects and Management

The user-reported list is short and mild. The animal findings are neither mild nor short, and they are the reason this section leads with them.

Cancer signal in rodentsNo human safe dose is established; exposure is the only lever you control
HeadacheReported by users; lower the dose if it persists
NauseaTake with food and reduce the dose
FatigueAdjust the timing of the daily tablet and review sleep
Thin human safety dataShort blocks and honest self-monitoring are the only realistic limits

No drug interactions are described in the sources, which is a statement about the absence of study rather than an assurance of safety. WADA issued explicit warnings about this compound, and anyone competing in a tested sport should assume the 40 day urinary window applies to them.

Store the pack in its original blister, at room temperature, out of direct sunlight and away from damp. The tablets are small and easy to lose, so keep them in the carton with the lot number rather than decanting them, and keep them somewhere children and pets cannot reach.

Because this is a research material with an unresolved safety profile, a tidy record matters more than usual: note the date the pack was opened and the date the block started, and dispose of any tablet that has discoloured or broken rather than using it.

Post-Cycle Therapy

There is no hormonal restart to plan, because this compound does not suppress the axis. What the end of a block needs is a health check rather than a protocol.

SERM restartNot applicable to this mechanism
Hormone panelOnly needed if a SARM was stacked alongside
General checksFull blood count, liver panel and lipids
Follow-upNo cardarine-specific biomarker of withdrawal exists
Cleaning timeUrine sulfone metabolites reported up to 40 days out

If a SARM was part of the same block, that compound sets the recovery rules, and a Nolvadex or Clomid protocol belongs to it rather than to the cardarine.

This listing states the strength, the tablet count and the manufacturer exactly as they ship, and it reports the 2007 rodent cancer findings and the WADA position instead of burying them, which is the least a research card should do. Orders go out discreetly, both international and US domestic pricing is shown on the product page before checkout, and every item is sold as a reference material rather than as a medicine. If cardarine is not the right fit, the rest of the Dragon Pharma line covers SARMs, peptides and recovery compounds, and our support team can confirm exactly what a listing contains before you order.

This page is educational and laboratory reference material. GW501516 is supplied as research-grade material for experimental work and is not offered as a medicine or as a treatment for any condition. The dosing figures restate non-medical practice where controlled human data does not exist, and the carcinogenicity signal from animal studies is reported as published. Nothing here is medical advice. Keep the product away from children and follow the regulations that apply where you live.
What is Cardarine (GW 501516)?
It is GW501516, a PPAR-delta agonist sold by Dragon Pharma as 20 mg tablets, 100 to a pack. The compound activates a nuclear receptor involved in fatty acid oxidation and oxidative metabolism in muscle, which is why it is discussed as an endurance and fat-loss agent. It is not an androgen, not a SARM and not an anabolic steroid.
Is Cardarine a SARM or a steroid?
Neither. SARMs bind the androgen receptor and steroids are androgens themselves, while Cardarine acts on PPAR-delta, a completely separate metabolic receptor. That difference explains the two things users care about most: no aromatisation and no water retention, but also no muscle-building signal at all, because there is nothing in the mechanism to build it.
What is the right Cardarine dosage?
Research and community material gives 10 mg a day for 8 weeks as the low end, 10-20 mg a day for 8-12 weeks as the working range, and 20 mg a day for up to 12 weeks as the ceiling. Above 20 mg there are no data, and the mouse and rat cancer study used 3 mg per kilogram per day, which is the only safety comparison that exists.
Does Cardarine cause cancer?
Cancer developed rapidly in several organs in mice and rats dosed at 3 mg per kilogram per day, and that finding is the reason development stopped. No equivalent human dataset exists, so the honest answer is that a risk is documented in animals and unquantified in people. Nothing in the reviewed sources supports calling it safe.
Why were Cardarine human trials stopped?
The programme was abandoned in 2007 after the animal carcinogenicity results appeared, before any long-term human safety work could be done. That is why so many rows on this card read Not established: the trial data were never generated, and later anti-doping warnings were issued on the strength of the animal findings.
Does Cardarine improve endurance?
The endurance reputation comes from animal studies in which large doses produced a large increase in working capacity. That is a real result in mice and rats and not a controlled human outcome, so the gap between the claim and the evidence is wide, and the same study line is where the cancer signal was found.
Do you need PCT after Cardarine?
No. There is no androgen activity and no suppression of natural testosterone production, so no tamoxifen or clomiphene restart belongs with this compound. If a suppressive SARM such as Ostarine or LGD 4033 was stacked in the same block, that SARM is what creates the recovery question.
Is Dragon Pharma Cardarine legit or are there fake batches around?
Counterfeit PPAR agonist tablets are common, so the pack itself is the first thing to check: sealed box, batch and expiry that match, an intact blister strip and a label stating 20 mg. Because the compound is inexpensive to press, an unusually low price is the usual warning sign, and a pack that cannot be traced should not be opened at all.

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