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the FDA has stated it lacks sufficient information to know whether the substance would cause harm when administered to humans Evidence snapshot: The evidence base is almost entirely preclinical, decades of animal (largely rat) studies, mostly from one Croatian research group (Sikiric et al., University of Zagreb), with a single small human trial under the brand name "Bepecin" (around 2015) that did not lead to any FDA-approved use

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[Abstract]2026 Mar 15;17(1):4002

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Pharmaceuticals 13:38 Herndon TM, Deisseroth A, Kaminskas E, Kane RC, Koti KM, Rothmann MD, Habtemariam B, Bullock J, Bray JD et al (2013) US Food and Drug Administration Approval: carfilzomib for the treatment of multiple myeloma FDA approval summary of carfilzomib

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