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Low-Density Lipoprotein Cholesterol–Lowering Effects of AMG 145, a Monoclonal Antibody to Proprotein Convertase Subtilisin/Kexin Type 9 Serine Protease in Patients With Heterozygous Familial Hypercholesterolemia
Author(s) -
Frederick J. Raal,
Robert C. Scott,
Ransi Somaratne,
Ian Bridges,
Gang Li,
Scott M. Wasserman,
Evan A. Stein
Publication year - 2012
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.112.144055
Subject(s) - medicine , familial hypercholesterolemia , pcsk9 , ezetimibe , endocrinology , statin , evolocumab , kexin , placebo , alirocumab , gastroenterology , compound heterozygosity , lipoprotein , cholesterol , ldl receptor , biochemistry , chemistry , mutation , pathology , alternative medicine , apolipoprotein a1 , gene
Despite statin treatment, many patients with heterozygous familial hypercholesterolemia do not reach desired low-density lipoprotein cholesterol (LDL-C) targets. AMG 145, a fully human monoclonal antibody against proprotein convertase subtilisin/kexin type 9 (PCSK9) serine protease, demonstrated significant reductions in LDL-C in phase 1 studies. This phase 2, multicenter, double-blind, randomized, placebo-controlled, dose-ranging study evaluated the efficacy and safety of AMG 145 in heterozygous familial hypercholesterolemia patients.

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