752-P: LIVRQNac (AXA1125) Enhances Insulin Sensitivity in Primary Human Hepatocytes and in Subjects with NAFLD and T2D

Background: AXA1125, an investigational composition of 5 amino acids and n-acetyl-cysteine, targets multiple biologies relevant to NAFLD pathogenesis. Methods: Primary human hepatocytes (PHH) from multiple donors were pretreated with AXA1125 components (LIVRQNac), exposed to lipotoxic insult in the...

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Veröffentlicht in:Diabetes (New York, N.Y.) N.Y.), 2021-06, Vol.70 (Supplement_1)
Hauptverfasser: BAUM, SETH, HARRISON, STEPHEN A., GUNN, NADEGE T., YOUNES, ZIAD, KOHLI, ANITA, PATIL, RASHMEE, FRIAS, JUAN P., HAMILL, MICHAEL, DAOU, NADINE, ZHAO, JEFF, CHAKRAVARTHY, MANU, KOZIEL, MARGARET
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Sprache:eng
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Zusammenfassung:Background: AXA1125, an investigational composition of 5 amino acids and n-acetyl-cysteine, targets multiple biologies relevant to NAFLD pathogenesis. Methods: Primary human hepatocytes (PHH) from multiple donors were pretreated with AXA1125 components (LIVRQNac), exposed to lipotoxic insult in the presence of LIVRQNac, incubated in high glucose insulin-free medium, followed by glucose-free medium±insulin. Human safety, tolerability, and biologic activity were evaluated in a 16-week, multicenter, randomized, placebo (Pbo)-controlled study (NCT04073368) in subjects with NAFLD±T2D. Results from Pbo and AXA1125 24 g twice daily dosing in subjects with T2D are reported. Results: In PHH, LIVRQNac reduced glucose output by ~50% (p
ISSN:0012-1797
1939-327X
DOI:10.2337/db21-752-P