Every protocol is prescription-based, reviewed by a licensed US provider, and compounded at a 503B-registered US pharmacy. See something you want — click to begin your consultation.
The gold standard of GLP-1 weight loss. Weekly subcutaneous injection that reduces appetite at the neurological level, drives sustained fat loss, and improves metabolic markers. Up to 15% body weight reduction in clinical trials.
Dual incretin receptor agonist targeting both GLP-1 and GIP receptors. Delivers superior weight loss compared to single GLP-1 agonists — up to 20%+ body weight reduction in trials. Once weekly injection.
Next-generation triple agonist. The most powerful weight loss peptide available — targeting GLP-1, GIP, and glucagon receptors simultaneously. Up to 24% body weight loss at 48 weeks in clinical studies.
A modified fragment of human growth hormone specifically targeting fat metabolism. Stimulates lipolysis and inhibits lipogenesis without the blood sugar effects of full HGH. Often stacked with GLP-1 protocols.
The recovery peptide elite athletes don't talk about publicly. 15-amino-acid sequence derived from gastric protein — accelerates healing of tendons, joints, muscles, and gut lining. Daily subcutaneous injection.
Systemic tissue repair through enhanced cell migration and angiogenesis. Reduces inflammation, accelerates wound healing, and improves flexibility. Particularly effective for chronic injuries and overuse conditions.
The most comprehensive recovery stack available. BPC-157 and TB-500 combined in one vial — synergistic healing of tendons, ligaments, muscles, and soft tissue. Stack and save vs. individual protocols.
Broad-spectrum antimicrobial peptide with immune-modulating properties. Supports wound healing, reduces bacterial loads, and strengthens immune defense. Particularly studied for chronic wounds and infections.
The gold standard starter growth hormone protocol. Stimulates your pituitary to produce natural GH — supporting body recomposition, recovery, energy, and sleep quality. Daily bedtime injection.
Selective GH release without cortisol or ACTH elevation. Supports lean muscle, fat metabolism, and recovery with minimal side effects. Often stacked with CJC-1295 for maximum effect.
The most popular growth hormone stack. CJC-1295 and Ipamorelin work synergistically — sustained GH and IGF-1 elevation through pulsatile release. Enhanced muscle, reduced fat, improved recovery and sleep.
Extended half-life of 6–8 days via DAC modification. Twice-weekly dosing for sustained GH and IGF-1 elevation — ideal for those preferring less frequent injections without sacrificing results.
FDA-approved for visceral fat reduction. Stimulates endogenous GH release targeting abdominal fat. Also studied for cognitive function in older adults. Daily injection with measurable results in 3–6 months.
Classic GH secretagogues that stimulate natural pulsatile GH release through the ghrelin receptor. Support body composition, recovery, and sleep quality. GHRP-6 notable for appetite stimulation.
The skincare industry's best-kept secret. GHK-Cu stimulates collagen and elastin synthesis, reverses skin thinning, and regenerates at the dermal level. Your skin, but pharmaceutical grade.
Our signature beauty protocol. GHK-Cu, BPC-157, and TB-500 in one vial — accelerated wound healing, skin rejuvenation, and tissue repair. Multi-system cellular renewal from the inside out.
The most comprehensive skin and tissue protocol. Adds KPV — a potent anti-inflammatory — to the Glow Blend. Collagen synthesis, tissue repair, inflammation control, and cellular renewal in one stack.
Stimulates natural melanogenesis for skin tanning and UV photoprotection without excessive sun exposure. Studied for vitiligo and erythropoietic protoporphyria. Fewer side effects than MT-II.
The essential coenzyme of cellular energy and DNA repair. NAD+ levels drop 50% by your 40s. Subcutaneous restoration drives mitochondrial function, mental clarity, and metabolic health. Feel the difference in days.
Activates telomerase to support telomere length and cellular longevity. Restores melatonin production, improves cardiovascular outcomes. Used in 20-day cycles twice yearly — the closest thing to a biological clock reset.
Mitochondrial-derived peptide that acts as a metabolic regulator through AMPK activation. Enhances insulin sensitivity, promotes fat oxidation, improves exercise capacity, and counters age-related metabolic decline.
Stabilizes mitochondrial membranes and optimizes the electron transport chain. Enhances ATP production, reduces oxidative stress. Demonstrated functional improvements in muscle strength and exercise capacity.
Selectively eliminates senescent "zombie" cells by disrupting FOXO4-p53 interaction. Improved physical fitness, organ function, and restored testosterone in aged models. Intermittent cycle protocol — 1 week on, 1 week off.
Enhances T-cell function and immune competence. Supports immunocompromised individuals and those dealing with chronic viral infections. Excellent safety profile with minimal side effects.
Enhanced anabolic signaling through extended IGF-1 activity. Supports protein synthesis, muscle development, and metabolic function. 8-week on / 4-week off cycling to prevent receptor desensitization.
Synthetic ACTH(4–10) analog developed in Russia. Supports attention, memory consolidation, and learning. Studied for stroke recovery and traumatic brain injury. Daily subcutaneous injection with gradual titration.
Acetylated form of Semax with enhanced stability and bioavailability. Same cognitive and neuroprotective benefits with potentially improved delivery. Once-daily subcutaneous administration.
Anxiolytic effects comparable to benzodiazepines — without sedation, dependence, or withdrawal. Anti-asthenic energy-boosting properties. Lasting neurobehavioral changes. 4 weeks on, 4 weeks off cycling.
Acetylated Selank with improved stability. Same anxiolytic and energy-boosting properties with potentially enhanced bioavailability. Daily subcutaneous with 4-week on/off cycling.
Naturally occurring nonapeptide that promotes deep, restorative slow-wave sleep. Stress-protective and anxiolytic properties. Does not induce pharmacological tolerance with continued use. Evening administration.
The bonding hormone — subcutaneous for systemic effects. Reduces anxiety, improves social connection, increases fat oxidation, and reduces caloric intake. Also studied for PTSD, depression, and addiction recovery.
FDA-approved for hypoactive sexual desire disorder (HSDD) in premenopausal women. Acts centrally — enhancing sexual desire through dopamine release in brain reward regions. On-demand, 45 minutes before activity.
Physiological sex hormone stimulation via LH/FSH signals without suppressing the HPG axis. Restores GnRH/LH pulsatility, resumes menstrual cycles in functional hypothalamic amenorrhea. Fertility and hormonal restoration.
Melanocortin receptor agonist promoting skin tanning without UV exposure. Also studied for libido enhancement in men and women. Loading phase followed by maintenance dosing. Use with caution — conservative dosing recommended.