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Home / Products / OSTARINA (MK-2866) · 20 MG · 60 TABLETAS | Modulador Selectivo. Rendimiento Avanzado. / OSTARINA (MK-2866) · 20 MG · 60 TABLETAS | Modulador Selectivo. Rendimiento Avanzado.
OSTARINA (MK-2866) · 20 MG · 60 TABLETAS | Modulador Selectivo. Rendimiento Avanzado.

Product Details

  • Technical Name: Ostarina (MK-2866) 20 mg, Comprimidos para Uso Humano
  • Laboratory / Brand: Kinetix Pharma
  • Active Ingredient (INN): Ostarina (MK-2866 Ostarine / Enobosarm)
  • Pharmaceutical Form: Comprimidos para Administración Oral
  • Concentration: 20 mg / Tablets
  • CAS Number: 841205-47-8
  • Internal SKU: SKU-OSTARINE-20MG-60TABS-841205478
Kinetix Pharma Ostarina (MK-2866 Ostarine / Enobosarm) Comprimidos para Administración Oral CAS: 841205-47-8
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OSTARINA (MK-2866) · 20 MG · 60 TABLETAS | Modulador Selectivo. Rendimiento Avanzado.

Muscle Growth Recovery Longevity & Performance

60 Servings Per Container: US$1.67 / serving

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US$99.99 USD
In stock (10,000 piece)
Ostarine (MK-2866) 20 mg tablets, from Kinetix Pharma, made in the Czech Republic. Each package contains 60 tablets of 20 mg each. This is a pharmaceutical-grade non-steroidal selective androgen receptor modulator (SARM) intended for human use. The active ingredient is ostarine (enobosarm), which promotes preservation and gain of lean muscle mass with unprecedented tissue selectivity. Used for muscle mass preservation during cutting and body recomposition cycles. CAS: 841205-47-8. Molecular formula: C₁₉H₁₄F₃N₃O₃. Store at room temperature in a dry place protected from light. WARNING: This product is an investigational compound and its use must be supervised by a physician. Banned by WADA. May cause hormonal axis suppression, transaminase elevation, and adverse effects on lipid profile.

Ostarine (MK-2866), also known as Enobosarm, is a next-generation non-steroidal selective androgen receptor modulator (SARM). Designed to mimic the anabolic action of testosterone in muscle and bone tissue, it promotes muscle growth and strength with unprecedented tissue selectivity. In the sports performance and research field, it is primarily used to preserve muscle mass during cutting phases or to promote lean tissue gains, maintaining high activity in muscle and bone.

The problem it solves: During intense training cycles or caloric restriction phases, athletes may experience muscle tissue loss. Ostarine, unlike traditional anabolic steroids, was developed to be selective with minimal impact on organs such as the prostate. Its targeted action profile makes it an advanced research tool for those seeking a more specific and potentially more favorable side effect profile.

Primary Benefit: Preservation and Gain of Lean Muscle Mass

At its core, Ostarine is designed to activate the androgen receptor (AR) with high affinity (Ki of 3.8 nM), activating pathways that promote protein synthesis in muscle. Its selective action seeks an anabolic effect in muscle and bone tissue, with less impact on tissues such as the prostate compared to testosterone. Recent clinical evidence demonstrates that Ostarine significantly preserves lean muscle mass, even in the context of GLP-1 drug-induced weight loss.

Secondary Benefits: Definition, Performance, and Recovery

Ostarine's action on the androgen receptor offers additional benefits:

Greater Muscle Definition: Ostarine does not aromatize to estrogen and does not cause the subcutaneous fluid retention typical of steroids, resulting in a drier, harder, and more vascular physique. Any weight gain is predominantly lean mass and intramuscular water (inside the muscle cell), not subcutaneous or extracellular bloating.

Enhanced Recovery: Users report noticeable improvements in recovery between training sessions, with increased muscle fullness and vascularity beginning to appear in week 2-3.

Osteoanabolic Effect: Ostarine has a positive effect on bone tissue, promoting bone formation and helping maintain bone mineral density, contributing to overall musculoskeletal health.

Pairing Strategy: Ostarine

Ostarine is typically used as a standalone agent for body recomposition or in cutting cycles. Cycling protocols vary according to goals: 8 weeks for an initial recomposition cycle (10-15 mg), 8-10 weeks for a classic cut (20-25 mg). Its use without an adequate post-cycle therapy (PCT) protocol is not recommended, especially at doses above 15 mg/day or cycles longer than 8 weeks.
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OSTARINA (MK-2866) · 20 MG · 60 TABLETAS | Modulador Selectivo. Rendimiento Avanzado.

Ostarine: Modulador Selectivo. Rendimiento Avanzado.

Para el atleta o investigador que busca maximizar la preservación de la masa muscular y lograr un físico definido y vascularizado, Ostarine representa la herramienta de modulación selectiva más avanzada. Este SARM no esteroideo promueve ganancias de tejido magro con un perfil de selectividad tisular sin precedentes, minimizando los efectos secundarios androgénicos y estrogénicos.

Beneficio Principal: Modulación Selectiva del Receptor Androgénico

Ostarine activa el receptor de andrógenos (AR) con alta afinidad. La evidencia clínica más reciente (2025-2026) y la experiencia en investigación han demostrado:

Preservación de la masa muscular magra durante la pérdida de peso.

Aumento de la fuerza y la recuperación muscular.

Mejora de la definición y vascularidad muscular.

Efecto positivo en la salud ósea.

Beneficios Adicionales: Rendimiento y Definición

Físico más Seco: Sin retención de líquidos, sin aromatización.

Mayor Definición: Músculos más duros y vascularizados.

Recuperación Acelerada: Reduce el tiempo entre sesiones de entrenamiento.

Sin Efectos Estrogénicos: No se aromatiza a estrógeno.

Ideal para Ciclos de Definición y Re-composición

Ostarine es la elección perfecta para ciclos de definición y recomposición corporal, donde el objetivo es perder grasa o re-componer el cuerpo sin sacrificar la masa muscular, logrando un físico seco, duro y extremadamente definido.

Key Benefits of Ostarine (MK-2866) Selective Androgen Receptor Modulation Ostarine is a next-generation non-steroidal selective androgen receptor modulator (SARM). Its molecular design confers high affinity for the androgen receptor (AR) in muscle and bone tissue (Ki of 3.8 nM), promoting protein synthesis and muscle growth with unprecedented tissue selectivity. Lean Muscle Mass Preservation Ostarine has been shown in recent clinical trials (2025) to significantly preserve lean muscle mass, even in the context of GLP-1 drug-induced weight loss such as semaglutide. This effect is especially valuable during cutting or caloric restriction cycles. Greater Muscle Definition and Vascularity By not aromatizing to estrogen, Ostarine prevents subcutaneous fluid retention, resulting in a drier, harder, and more vascular physique. Any weight gain is predominantly lean mass and intramuscular water, not subcutaneous bloating. Enhanced Recovery Users report noticeable improvements in recovery between training sessions, with increased muscle fullness and vascularity beginning to appear in week 2-3. Strength in compound movements also shows progress during this period. Osteoanabolic Effect Ostarine has a positive effect on bone tissue, promoting bone formation and helping maintain bone mineral density. This effect contributes to overall musculoskeletal health. No Estrogenic Effects As it is not a steroid, Ostarine is not a substrate for the aromatase enzyme, so it is not converted to estradiol. This eliminates the risks of gynecomastia, fluid retention, and other estrogenic side effects associated with traditional anabolic steroids.
Function and Mechanism of Action of Ostarine (MK-2866) Ostarine (MK-2866), also known as Enobosarm, is a next-generation non-steroidal selective androgen receptor modulator (SARM). It was originally developed for the treatment of muscle wasting in chronic diseases and has been adapted for use in sports performance research. Detailed Mechanism of Action: Androgen Receptor Activation: Ostarine binds to the androgen receptor (AR) with high affinity (Ki of 3.8 nM), even greater than testosterone in some tissues. This binding initiates gene transcription that promotes protein synthesis and muscle growth. Tissue Selectivity: Its molecular design seeks an anabolic effect in muscle and bone tissue, with less impact on tissues such as the prostate compared to testosterone. This selectivity is the basis of its potentially more favorable side effect profile. Protein Synthesis and Nitrogen Retention: Ostarine increases the efficiency with which the body uses proteins to build muscle tissue, resulting in a positive nitrogen balance, a necessary condition for muscle growth and preservation. Absence of Estrogenic Activity: As it is not a steroid, Ostarine is not a substrate for the aromatase enzyme, so it is not converted to estradiol. This eliminates the risks of gynecomastia, fluid retention, and other estrogenic side effects. Half-Life: It has a half-life of approximately 24 hours, allowing for stable dosing in research protocols and single daily administration. Recent Clinical Evidence (2025-2026): Ostarine has been shown in Phase 2b clinical trials (QUALITY, 2025) to significantly preserve lean muscle mass in GLP-1 treated patients, with fat reduction and improvement in physical function. Veru has announced plans to initiate Phase 3 trials in 2026.
How to Use Ostarine (MK-2866) Route of Administration: Oral. Ostarine is administered as tablets for oral ingestion. Tablets should be swallowed whole with water. Dosage: Dosage should be determined by a physician or researcher according to indications and patient condition. General dosage guidelines for Ostarine include: Initial Cycle / Cautious Recomp: 10-15 mg per day for 8 weeks. Classic Cut Cycle: 20-25 mg per day for 8-10 weeks. Aggressive Cut Cycle (Experienced): 25-30 mg per day for 10-12 weeks. Female Protocol: 5-10 mg per day for 8-10 weeks for recomp. Frequency: Daily administration. Ostarine has a half-life of approximately 24 hours, allowing for single daily administration to maintain stable blood levels. Treatment Duration: For cutting or recomposition cycles, 8-10 week cycles are recommended. Prolonged use may result in hormonal axis suppression. Post-Cycle Therapy (PCT): A mini-PCT is recommended after any Ostarine cycle, especially at doses above 15 mg/day or cycles longer than 8 weeks. Common protocols include: - Enclomiphene 12.5 mg/day for 3-4 weeks - Tamoxifen (Nolvadex) 20/20/10/10 mg for 4 weeks - Clomiphene (Clomid) 25 mg/day for 4 weeks Storage: Store in a cool, dry place, protected from light and at room temperature. Keep out of reach of children. Important Notice: Product intended FOR HUMAN USE under medical supervision or for research use. Ostarine is an investigational compound and its use must be supervised by a professional. May cause hormonal axis suppression, transaminase elevation (ALT/AST), and adverse effects on lipid profile. Not recommended for individuals with liver disease, cardiovascular disease, or in pregnant women.
Ingredients of Ostarine (MK-2866) Active Ingredient: Ostarine (MK-2866 / Enobosarm): A next-generation non-steroidal selective androgen receptor modulator (SARM) that promotes preservation and gain of lean muscle mass with unprecedented tissue selectivity. Molecular formula: C₁₉H₁₄F₃N₃O₃. Molecular weight: 389.33 g/mol. CAS: 841205-47-8. Alternative names: Enobosarm, GTx-024, VERU-024. Excipients: Each 20 mg tablet contains the following excipients (according to standard Ostarine formulations): Lactose monohydrate: Used as an excipient and bulking agent. Microcrystalline cellulose: Used as a bulking agent and disintegrant. Corn starch: Used as a disintegrant and bulking agent. Magnesium stearate: Used as a lubricant. Colloidal anhydrous silica: Used as a flow agent. Note: Specific excipients may vary by manufacturer. Consult the product leaflet for the complete list of excipients. Note for Users: This product is a pharmaceutical-grade compound manufactured under strict quality control standards (GMP) by Kinetix Pharma, in the Czech Republic. Each package contains 60 tablets of 20 mg each.
Onset Time & Expected Results of Ostarine (MK-2866) Onset of Action (Week 1): Ostarine begins to reach steady state in blood during the first week due to its 24-hour half-life. Most users do not notice significant effects during the first week, although some report subtle improvements in recovery and mood by the end of the week. Measurable Benefits (Weeks 2-3): Noticeable improvements in recovery between training sessions. Increased muscle fullness and vascularity, particularly in users with low body fat percentage. Strength gains in compound movements may become apparent. Some users report improved joint comfort. Full Effect (Weeks 6-8): Peak effects are realized. Typical lean mass gains are 2-4 kg at doses of 15-25 mg. Body fat reduction is noticeable in those training and eating for recomposition. Some degree of HPTA suppression is expected, particularly at doses above 20 mg. Projected Results (12-week cycle): On a 12-week cycle with Ostarine, projected lean mass gains are 3.4-5.7 lbs (1.5-2.6 kg) and fat loss of 2.1-3.4 lbs (0.95-1.5 kg) in males. Factors Influencing Results: The speed and magnitude of results depend on dose administered, adherence to the cycling protocol, nutrition quality, caloric deficit or surplus, training type, and individual metabolism.
Clinical Research & 3rd Party Test Results / Clinical Research & 3rd Party Test Results - 🇺🇸 English Clinical Research & 3rd Party Test Results of Ostarine (MK-2866) The most recent scientific evidence on Ostarine (Enobosarm) comes from decades of clinical research and recent trials in 2025-2026. Recent Clinical Evidence (2025-2026): Phase 2b QUALITY Trial (2025): Ostarine (Enobosarm) demonstrated significant preservation of lean muscle mass in patients treated with GLP-1 receptor agonists (Wegovy/semaglutide) for weight loss. The trial met its primary endpoint, showing statistically significant protection of total lean body mass compared to placebo. Key secondary endpoints showed superior total fat mass reduction and preservation of physical function (stair-climbing power). Based on these results, Veru plans to initiate Phase 3 trials in 2026. Phase 2 Trial in Elderly (2013): A 12-week trial in 120 healthy elderly men and postmenopausal women showed dose-dependent increases in total lean body mass (1-3 mg doses) and improvements in physical function. Molecular Binding Studies (2025): Computational and in vitro studies have demonstrated that Ostarine binds to the androgen receptor with high affinity (Ki of 3.8 nM). Advanced molecular dynamics simulations confirmed stable binding to the AF-1 region of the AR protein. Safety Considerations: Common Side Effects: Testosterone suppression (dose-dependent, typically 10-30% reduction at 25 mg), HDL cholesterol reduction (10-20% suppression observed in clinical trials), headaches during the first 1-2 weeks, transient fatigue toward the end of longer cycles, and slight reduction in libido at higher doses. Serious Side Effects: Liver enzyme elevations (ALT elevations documented in 6.7-20.8% of clinical trial participants), potential for clinically apparent liver injury with jaundice (case reports, typically in high-dose or stacking scenarios), myocardial infarction, stroke, hallucinations, psychotic-like behaviors, and severe sexual dysfunction. Contraindications: Individuals under 21 years of age (risk of premature HPTA disruption), known hypersensitivity to MK-2866 or any formulation excipients, pregnancy and breastfeeding, and pre-existing liver or cardiovascular disease. Regulatory Status: Ostarine is not approved by the FDA for human use in the United States. It is classified as a banned substance by the World Anti-Doping Agency (WADA) and the International Olympic Committee (IOC). The FDA has issued warning letters to companies selling SARMs, including Ostarine (December 2025), emphasizing significant safety concerns including liver toxicity and increased risk of heart attack and stroke. Kinetix Pharma Quality Standards: Pharmaceutical Grade: Pharmaceutical-grade compound for human use or research. Manufacturing: Manufactured in the Czech Republic under strict GMP standards by Kinetix Pharma. Quality Control: Each batch is subjected to quality control testing to ensure purity and potency.

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