4.6 Article

Rationale and design of two trials assessing the efficacy, safety, and tolerability of inclisiran in adolescents with homozygous and heterozygous familial hypercholesterolaemia

Journal

EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY
Volume 29, Issue 9, Pages 1361-1368

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/eurjpc/zwac025

Keywords

Hyperlipoproteinaemia type II; Cholesterol; LDL; Proprotein convertase 9; Inclisiran; RNA; Small interfering; Double-blind method; Paediatric; Adolescent

Funding

  1. Novartis Pharma AG

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Inclisiran is a promising new therapeutic option for lowering LDL-C levels in adults with atherosclerotic cardiovascular disease, and ongoing studies are investigating its efficacy, safety, and tolerability in adolescents diagnosed with familial hypercholesterolaemia. The trials aim to assess the impact of Inclisiran in adolescents with homozygous or heterozygous familial hypercholesterolaemia, with primary endpoints focused on changes in LDL-C levels over time.
Background Inclisiran is a small interfering RNA molecule that reduces low-density lipoprotein cholesterol (LDL-C) by inhibition of proprotein convertase subtilisin/kexin type 9. This subcutaneous, twice-yearly administered agent has been shown to effectively and safely lower LDL-C in adult patients with established atherosclerotic cardiovascular disease, adults at high risk for atherosclerotic cardiovascular disease, as well as in adults with heterozygous familial hypercholesterolaemia. With the current, limited treatment options available to reach treatment goals in children with severe heterozygous familial hypercholesterolaemia, homozygous familial hypercholesterolaemia, or statin intolerance, inclisiran could be a valuable new therapeutic option. Objectives The objective of these ongoing studies is to investigate the efficacy, safety, and tolerability of inclisiran in adolescents diagnosed with homozygous familial hypercholesterolaemia (ORION-13) or heterozygous familial hypercholesterolaemia (ORION-16). Study design ORION-13 and ORION-16 are both two-part (1-year double-blind inclisiran vs. placebo/1 year open-label inclisiran) multicentre trials including adolescents aged 12 to <18 years diagnosed with familial hypercholesterolaemia. ORION-13 will include similar to 12 participants diagnosed with homozygous familial hypercholesterolaemia and ORION-16 will include similar to 150 participants diagnosed with heterozygous familial hypercholesteroleamia. The primary endpoint is the percentage change in LDL-C from baseline to Day 330. Secondary efficacy and safety endpoints include changes in other lipid parameters and treatment-emergent adverse events as well as laboratory parameters and vital signs. Exploratory endpoints include individual responsiveness of the participants and change in LDL-C according to the type of underlying causal mutation.

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