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Oral doses used in animal studies are typically three to ten times higher than equivalent injectable doses to produce comparable systemic effects suggesting oral bioavailability in the range of 1030% relative to parenteral delivery.3 That does not mean oral BPC-157 is ineffective

Furthermore, (-)-Vestitol has been identified as an -glucosidase inhibitor and can bind to the PPAR- receptor, suggesting potential therapeutic effects for diabetes mellitus [39, 40]

What the Evidence Suggests (So Far) Tendon & musculoskeletal: In vitro work shows BPC-157 can increase growth-hormone receptor expression in tendon fibroblasts, consistent with tissue repair pathways