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It involves the nonenzymatic conversion of asparagine and glutamine residues to their corresponding acidic forms (aspartate and glutamate)

Journal of Biomaterials Science, Polymer Edition , 2008

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Protocol overview: BPC-157 administered via subcutaneous injection, locally near the affected joint Standard dosing range: 200500 mcg per injection session Treatment duration: 48 weeks of active treatment Follow-up assessments: 6 months and 12 months post-treatment Patients were evaluated using validated pain scales (VAS and KOOS scores) and functional mobility assessments at each follow-up point