Journal article

Efficacy and safety of maralixibat treatment in patients with Alagille syndrome and cholestatic pruritus (ICONIC): a randomised phase 2 study

E Gonzales, W Hardikar, M Stormon, A Baker, L Hierro, D Gliwicz, F Lacaille, A Lachaux, E Sturm, KDR Setchell, C Kennedy, A Dorenbaum, J Steinmetz, NK Desai, AJ Wardle, W Garner, P Vig, T Jaecklin, EM Sokal, E Jacquemin

Lancet | Published : 2021

Abstract

Background: Alagille syndrome is a rare genetic disease that often presents with severe cholestasis and pruritus. There are no approved drugs for management. Maralixibat, an apical, sodium-dependent, bile acid transport inhibitor, prevents enterohepatic bile acid recirculation. We evaluated the safety and efficacy of maralixibat for children with cholestasis in Alagille syndrome. Methods: ICONIC was a placebo-controlled, randomised withdrawal period (RWD), phase 2b study with open-label extension in children (aged 1–18 years) with Alagille syndrome (NCT02160782). Eligible participants had more than three times the normal serum bile acid (sBA) levels and intractable pruritus. After 18 weeks o..

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University of Melbourne Researchers