Evinacumab for Homozygous Familial Hypercholesterolemia
Эвинакумаб при гомозиготной семейной гиперхолестеринемии
2020-08-20
SCID: 54.1/7wtbpxqd
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ELIPSE HoFH TrialEvinacumabHomozygous familial hypercholesterolemiaLDL cholesterol reductionRegeneron NCT03399786
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Abstract (AI)
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.).
Key Findings
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.
Research Object
Evinacumab therapy in patients with homozygous familial hypercholesterolemia receiving maximal lipid-lowering therapy
Research Subject
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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