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If a patient were to suffer an adverse outcome potentially linked to BPC-157, the physician could be found liable for using an unauthorized treatment

on uremic pruritus in hemodialysis patients: a randomized, double-blind, placebo-controlled trial

Specifically, eligible studies included participants (P) with a confirmed diagnosis of vitamin B12 deficiency, interventions (I) involving oral or sublingual vitamin B12 administration, comparators (C) using intramuscular supplementation, and outcomes (O) reporting changes in serum vitamin B12 or homocysteine levels

The critical distinction with AOD-9604 is its complete lack of effect on IGF-1 levels