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Research & Educational Use Only. This protocol guide is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional before beginning any research protocol.
PPARdelta Agonist Evidence Grade: C+ (Abandoned Phase II)

GW-501516 (Cardarine) Protocol Guide

⚠ No validated human dose. This compound is not FDA-approved and has no peer-reviewed human dose-finding trials. The figures below are research conventions extrapolated from preclinical (animal/in‑vitro) and community sources — not validated clinical dosing. Treat them as study references only. Research use only; not medical advice.

GW-501516 (Cardarine) is a selective PPARdelta receptor agonist developed by GlaxoSmithKline. It dramatically enhances endurance, fat oxidation, and lipid metabolism. Development was abandoned after animal studies showed cancer at extreme doses. It is not a SARM.

Protocol Overview

Compound
GW-501516 (Cardarine / Endurobol)
Category
PPARdelta Receptor Agonist (Metabolic Modulator)
Mechanism
Activates PPARdelta, shifting cellular energy metabolism from glucose to fatty acid oxidation. Upregulates fat-burning genes, increases mitochondrial biogenesis, improves lipid profile (HDL up, LDL and triglycerides down), and dramatically enhances endurance capacity
Half-Life
16-24 hours
Form
Oral liquid or capsule
Route
Oral
Frequency
Once daily
Cycle Length
8-12 weeks

Dosing Protocol

ProtocolDoseFrequencyRouteDuration
Standard10 mg1x dailyOral8 weeks
Enhanced15 mg1x dailyOral8-10 weeks
Maximum20 mg1x dailyOral8-12 weeks

Expected Timeline

Week 1-2
Enhanced endurance within days. Ability to sustain cardiovascular exercise significantly increased.
Week 3-4
Major endurance and fat loss effects. Lipid panel improves (HDL increase, triglycerides decrease).
Week 5-6
Peak fat loss effects. Body composition changes clearly visible. Endurance at maximum enhancement.
Week 7-8
Continued benefits. Lipid profile significantly improved. Good stopping point for standard cycle.
Week 9-12
Extended cycle for experienced users. No hormonal suppression to manage.

Side Effects & Monitoring

Common Side Effects

  • Generally very well tolerated at standard doses
  • Rare headaches
  • Occasional mild GI discomfort
  • Potential for increased appetite

Precautions

  • Cancer concerns: rodent studies showed tumor development at high doses over 2 years
  • No long-term human safety data
  • Does not suppress testosterone - no PCT needed
  • Banned by WADA for athletic competition
  • Individual risk assessment essential given cancer data

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Frequently Asked Questions

Is Cardarine safe given the cancer concerns?

The cancer risk is debated. Rodent studies used doses far exceeding typical human use (100x+) for extended periods. No human cancer data exists. However, the lack of long-term human safety data means the risk cannot be definitively quantified.

Does Cardarine suppress testosterone?

No. GW-501516 does not interact with androgen receptors or the HPTA axis. No PCT is needed. It is commonly stacked with SARMs because it adds endurance and fat loss without additional suppression.

How quickly does Cardarine work?

Many users report noticeable endurance improvement within 1-3 days of first dose. The effect on cardio capacity is often described as dramatic. Fat loss effects build over several weeks.

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⚠ Before any use: human safety data is limited or absent for many of these compounds. Consult a licensed healthcare provider first — especially if you are pregnant or nursing, have a medical condition, or take other medications.