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Until human clinical trials (the kind the FDAs July 2026 PCAC consultation is partly designed to assess the case for) produce safety and efficacy data in actual populations of users, the gap between what BPC-157 might do and what is documented that it does in people remains the most important thing to understand about it.
As with any IV therapy, vascular access, strict sterility, and the small but real possibility of an allergic or anaphylactic reaction apply
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