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Efficacy and Safety of Alirocumab in Adults With Homozygous Familial Hypercholesterolemia

Open access
Blom, Dirk J., Harada-Shiba, Mariko, Rubba, Paolo, Gaudet, Daniel, Kastelein, John J.P., Charng, Min-Ji, Pordy, Robert, Donahue, Stephen, Ali, Shazia, Dong, Yuping, Khilla, Nagwa, Banerjee, Poulabi, Baccara-Dinet, Marie, Rosenson, Robert S.·2020·Journal of the American College of Cardiology

Abstract

BACKGROUND: Homozygous familial hypercholesterolemia (HoFH) is characterized by extremely elevated low-density lipoprotein-cholesterol (LDL-C) levels and early onset atherosclerotic cardiovascular disease despite treatment with conventional lipid-lowering treatment. OBJECTIVES: This study was designed to assess LDL-C reduction with the proprotein convertase subtilisin/kexin type 9 inhibitor alirocumab in adult patients with HoFH. METHODS: This randomized, double-blind, placebo-controlled, parallel-group, phase 3 study evaluated efficacy and safety of alirocumab 150 mg every 2 weeks. The primary endpoint was percent reduction from baseline in LDL-C versus placebo after 12 weeks of treatment. RESULTS: Patients (N = 69) were randomized 2:1 to alirocumab or placebo. At baseline, background lipid-lowering treatment included 67 patients receiving statin (59 patients on high-intensity statin); 50 patients on ezetimibe; 10 patients on lomitapide; and 10 patients undergoing apheresis. Mean baseline LDL-C was 259.6 mg/dl in the placebo group and 295.0 mg/dl in the alirocumab group. At week 12, the least squares mean difference in LDL-C percent change from baseline was -35.6% (alirocumab [-26.9%] vs. placebo [8.6%]; p < 0.0001). Reductions (least squares mean difference) in other atherogenic lipids at week 12 were: apolipoprotein B, -29.8%; non-high-density lipoprotein cholesterol, -32.9%; total cholesterol, -26.5%; and lipoprotein(a), -28.4% (all p < 0.0001). No serious adverse events, permanent treatment discontinuations, or deaths due to treatment-emergent adverse events were reported during the double-blind treatment period. CONCLUSIONS: In the largest randomized controlled interventional trial in HoFH patients to date, alirocumab resulted in significant and clinically meaningful reductions in LDL-C at week 12. Alirocumab was generally well tolerated, with a safety profile comparable to that of placebo. (Study in Participants With Homozygous Familial Hypercholesterolemia [HoFH] [ODYSSEY HoFH] NCT03156621.).

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Metadata

Authors
Blom, D. J., Harada-Shiba, M., Rubba, P., Gaudet, D., Kastelein, J. J. P., Charng, M.-J., Pordy, R., Donahue, S., Ali, S., Dong, Y., Khilla, N., Banerjee, P., Baccara-Dinet, M., & Rosenson, R. S.
Venue
Journal of the American College of Cardiology
Publisher
Elsevier BV
Published
2020-07
Volume
76
Issue
2
Pages
131-142
ISSN
0735-1097 (ISSN-L)
OpenAlex
W3039823791
Cited by
166
References
4
FWCI
19.92
Type
journal article
Language
en
Open access
hybrid

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Blom, D. J., Harada-Shiba, M., Rubba, P., Gaudet, D., Kastelein, J. J. P., Charng, M.-J., Pordy, R., Donahue, S., Ali, S., Dong, Y., Khilla, N., Banerjee, P., Baccara-Dinet, M., & Rosenson, R. S. (2020). Efficacy and Safety of Alirocumab in Adults With Homozygous Familial Hypercholesterolemia. Journal of the American College of Cardiology. https://doi.org/10.1016/j.jacc.2020.05.027

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