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Selank for Attenuating Neurotoxicity and Substance Withdrawal Preclinical and clinical research indicates that Selank may possess neuroprotective effects to attenuate withdrawal symptoms following the abuse of addictive substances

You may be eligible if you: Are aged 18 or older, either with or without type 2 diabetes, with a BMI of 27 or greater Have been diagnosed with chronic kidney disease Either have an eGFR between 25-60, or an eGFR between 25-75 with a UACR of more than 30 Have been receiving an angiotensin-converting enzyme (ACE) or angiotensin II receptor blockers (ARB) that is considered the maximum appropriate dose for treatment of chronic kidney disease or hypertension (unless the participant has low blood pressure or hypotension) Have an A1C of below 6.5 (if you do not have type 2 diabetes) Have an A1C of below 9.5 (if you do have type 2 diabetes), as well as a diabetes diagnosis that occurred more than 180 days prior to screening People who have lost or gained more than 11 pounds (5 kg) within 90 days of screening, people with type 1 diabetes, and people who have had or plan to have bariatric surgery or device-based therapy for obesity may not be eligible to participate

Syringe Units = Volume to Draw (mL) 100 = 0.4 mL 100 = 40 units Tesamorelin Dosing Profile (10 mg Vial / 2 mL BAC Water) 1 mg Dose: Draw 20 units (0.2 mL)

Copper peptides work best on areas where follicles are still present but dormant or miniaturized

Nature 443 (7109), 289295 (2006)