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BPC-157 protocols often specify injection proximity to the affected tendon or joint
10.1002/term.2841 42 ChenW.-J.TsaiT.-T.ChenL.-H.NiuC.-C.LaiP.-L.FuT.-S.et al (2005)
Most clinical studies assess outcomes at 24 weeks, with continued improvement typically observed through 12 to 24 months of use
Anti-Doping Agency (USADA) Wada-Ama Low risk because natural gastric derivative (fallacy: synthetic product with limited human PK and impurity concerns)
