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Oral delivery via PepT1: Published research (Dalmasso et al., 2008, Gastroenterology ) demonstrated that KPV can be absorbed through the PepT1 intestinal peptide transporter, enabling oral administration extremely unusual for a therapeutic peptide
Preclinical studies showed no adverse effects across several organ systems including liver, spleen, lung, kidney, brain, thymus, prostate, and ovaries in studies up to 6 weeks
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