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Description

BPC-157 works by promoting tissue repair and reducing inflammation

One of its most common hereditary forms, spinocerebellar ataxia type 3 (SCA3), stems from a genetic mutation in the ATXN3 gene and progressively damages the cerebellum

Thymosin beta-4 faculty publications

Human clinical research remains early stage, with small pilot studies exploring its effects on exercise performance, insulin sensitivity, and metabolic biomarkers rather than obesity endpoints