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BPC-157 has more structured preclinical toxicology behind it than the TB-500 fragment does, but neither has the long-duration and carcinogenicity data that a safety conclusion would require, and the human evidence that does exist for the TB-500 label actually belongs to a different, pharmaceutical-grade molecule

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Top-line outcomes at the 48-week primary endpoint, by dose: Secondary endpoint magnitudes at the 12mg cohort: approximately 41% mean reduction in fasting insulin

doi: 10.1016/j.freeradbiomed.2015.06.011 30 ParvezS.KangM.ChungH