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Inclisiran for the Treatment of Heterozygous Familial Hypercholesterolemia
Author(s) -
Frederick J. Raal,
David Kallend,
Kausik K. Ray,
Traci Turner,
Wolfgang Köenig,
R. Scott Wright,
Peter Wijngaard,
Danielle Curcio,
Mark Jaros,
Lawrence A. Leiter,
John J.P. Kastelein
Publication year - 2020
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1913805
Subject(s) - familial hypercholesterolemia , medicine , pcsk9 , placebo , cholesterol , endocrinology , confidence interval , gastroenterology , lipoprotein , ldl receptor , alternative medicine , pathology
Familial hypercholesterolemia is characterized by an elevated level of low-density lipoprotein (LDL) cholesterol and an increased risk of premature atherosclerotic cardiovascular disease. Monoclonal antibodies directed against proprotein convertase subtilisin-kexin type 9 (PCSK9) have been shown to reduce LDL cholesterol levels by more than 50% but require administration every 2 to 4 weeks. In a phase 2 trial, a twice-yearly injection of inclisiran, a small interfering RNA, was shown to inhibit hepatic synthesis of PCSK9 in adults with heterozygous familial hypercholesterolemia.

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