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They may, however, exhibit slower onset and potentially slightly less systemic bioavailability compared to a clean injection

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Patients with hepatic impairment present two competing considerations

BPC-157 would still require a full New Drug Application (NDA) supported by adequate human clinical trials to achieve formal FDA approval

Wei Wang, [email protected] These authors have contributed equally to this work Disclaimer All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers