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This approach demonstrated high feasibility for early in vivo diagnosis of ACI/AKI, detecting these conditions at least 24 and 48 hours earlier than standard clinical assays for ACI and AKI, respectively

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Di Marzio L, Moretti S, D'Alo S, Zazzeroni F, Marcellini S, Smacchia C, Alesse E, Cifone MG, De Simone C

In fact, the FDA designated BPC-157 as a Category 2 bulk drug substance, meaning it cannot be compounded by commercial pharmaceutical companies due to insufficient safety evidence in humans

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