Evinacumab for Homozygous Familial Hypercholesterolemia

Эвинакумаб при гомозиготной семейной гиперхолестеринемии
John J.P. Kastelein, George D. Yancopoulos, G. Kees Hovingh, Frederick J. Raal, Robert Pordy, Daniel Gaudet, Poulabi Banerjee, Robert S. Rosenson, Laurens F. Reeskamp, Paolo Rubba, Shazia Ali, Kuo‐Chen Chan, Daniel A. Gipe, Nagwa Khilla, David M. Weinreich, Yi Zhang
2020-08-20

ELIPSE HoFH TrialEvinacumabHomozygous familial hypercholesterolemiaLDL cholesterol reductionRegeneron NCT03399786
BACKGROUND: ) are associated with hypolipidemia and protection against atherosclerotic cardiovascular disease. Evinacumab, a monoclonal antibody against ANGPTL3, has shown potential benefit in patients with homozygous familial hypercholesterolemia. METHODS: In this double-blind, placebo-controlled, phase 3 trial, we randomly assigned in a 2:1 ratio 65 patients with homozygous familial hypercholesterolemia who were receiving stable lipid-lowering therapy to receive an intravenous infusion of evinacumab (at a dose of 15 mg per kilogram of body weight) every 4 weeks or placebo. The primary outcome was the percent change from baseline in the LDL cholesterol level at week 24. RESULTS: The mean baseline LDL cholesterol level in the two groups was 255.1 mg per deciliter, despite the receipt of maximum doses of background lipid-lowering therapy. At week 24, patients in the evinacumab group had a relative reduction from baseline in the LDL cholesterol level of 47.1%, as compared with an increase of 1.9% in the placebo group, for a between-group least-squares mean difference of -49.0 percentage points (95% confidence interval [CI], -65.0 to -33.1; P<0.001); the between-group least-squares mean absolute difference in the LDL cholesterol level was -132.1 mg per deciliter (95% CI, -175.3 to -88.9; P<0.001). The LDL cholesterol level was lower in the evinacumab group than in the placebo group in patients with null-null variants (-43.4% vs. +16.2%) and in those with non-null variants (-49.1% vs. -3.8%). Adverse events were similar in the two groups. CONCLUSIONS: In patients with homozygous familial hypercholesterolemia receiving maximum doses of lipid-lowering therapy, the reduction from baseline in the LDL cholesterol level in the evinacumab group, as compared with the small increase in the placebo group, resulted in a between-group difference of 49.0 percentage points at 24 weeks. (Funded by Regeneron Pharmaceuticals; ELIPSE HoFH ClinicalTrials.gov number, NCT03399786.).
1
Evinacumab produced a 49.0 percentage-point greater reduction in LDL cholesterol versus placebo at 24 weeks in homozygous familial hypercholesterolemia patients on maximal lipid-lowering therapy.
2
Placebo-treated patients had a small increase in LDL cholesterol over 24 weeks while evinacumab-treated patients had a substantial reduction.
3
The study population consisted of patients with homozygous familial hypercholesterolemia receiving maximum doses of lipid-lowering therapy.

Evinacumab therapy in patients with homozygous familial hypercholesterolemia receiving maximal lipid-lowering therapy

Effect of evinacumab on reduction in LDL cholesterol level (percentage change from baseline at 24 weeks) compared with placebo

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2020-08-20
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John J.P. Kastelein
George D. Yancopoulos
G. Kees Hovingh
Frederick J. Raal
Robert Pordy
Daniel Gaudet
Poulabi Banerjee
Robert S. Rosenson
Laurens F. Reeskamp
Paolo Rubba
Shazia Ali
Kuo‐Chen Chan
Daniel A. Gipe
Nagwa Khilla
David M. Weinreich
Yi Zhang
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