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Anyone seeking a regulated medical treatment BPC-157 is not an FDA-approved drug

2017], another confirmatory phase III placebo-controlled trial showed that edaravone treatment resulted in a statistically significant change in ALS FRS-R primary endpoint over 24 weeks in a subset of ALS patients (2017

& Shevde, L

References: Kang et al

Rats receiving BPC-157 at doses of 10 micrograms or 10 nanograms per kilogram showed improvement across every measured outcome: clinical recovery, microscopic nerve architecture, morphometric analysis, electromyography (EMG), and functional walking recovery measured by the sciatic functional index