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BPC-157 is not FDA-approved for human therapeutic use and is classified as a Category 2 bulk drug substance by the FDA

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72 For treatment of genotype 4, the SYNERGY trial demonstrated an SVR rate of 95% by intention to treat analysis following 12 weeks of ledipasvir/sofosbuvir therapy

TB-500 dosage is fundamentally different from most peptides - this is not a daily microdose compound

Lipid droplet-derived monounsaturated fatty acids traffic via PLIN5 to allosterically activate SIRT1