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Zhang, S., Liu, H., Yu, H

doi: 10.1159/000209979 7 Cantero-NavarroERayego-MateosSOrejudoMTejedor-SantamariaLTejera-MuozASanzABet al

Retrieved 8 January 2025

Researchers designing preclinical BPC-157 protocols should account for these data limitations in their risk assessments and experimental designs, include appropriate monitoring endpoints informed by the peptides known NO-dependent mechanism, and contribute to the expansion of the preclinical safety database through systematic collection and reporting of safety-relevant endpoints

For a long-form Australian-context explainer of how Schedule 4 status interacts with the Personal Importation Scheme, what FDA reclassification means and does not mean, and what "research-only" framing looks like under the Therapeutic Goods Act, see /blog/is-bpc-157-legal-in-australia-2026