» Articles » PMID: 38856678

Evinacumab in Homozygous Familial Hypercholesterolaemia: Long-term Safety and Efficacy

Abstract

Background And Aims: Homozygous familial hypercholesterolaemia (HoFH) is a rare genetic disorder characterized by severely elevated LDL cholesterol (LDL-C) and premature atherosclerotic cardiovascular disease. In the pivotal Phase 3 HoFH trial (NCT03399786), evinacumab significantly decreased LDL-C in patients with HoFH. This study assesses the long-term safety and efficacy of evinacumab in adult and adolescent patients with HoFH.

Methods: In this open-label, single-arm, Phase 3 trial (NCT03409744), patients aged ≥12 years with HoFH who were evinacumab-naïve or had previously received evinacumab in other trials (evinacumab-continue) received intravenous evinacumab 15 mg/kg every 4 weeks with stable lipid-lowering therapy.

Results: A total of 116 patients (adults: n = 102; adolescents: n = 14) were enrolled, of whom 57 (49.1%) were female. Patients were treated for a median (range) duration of 104.3 (28.3-196.3) weeks. Overall, treatment-emergent adverse events (TEAEs) and serious TEAEs were reported in 93 (80.2%) and 27 (23.3%) patients, respectively. Two (1.7%) deaths were reported (neither was considered related to evinacumab). Three (2.6%) patients discontinued due to TEAEs (none were considered related to evinacumab). From baseline to Week 24, evinacumab decreased mean LDL-C by 43.6% [mean (standard deviation, SD), 3.4 (3.2) mmol/L] in the overall population; mean LDL-C reduction in adults and adolescents was 41.7% [mean (SD), 3.2 (3.3) mmol/L] and 55.4% [mean (SD), 4.7 (2.5) mmol/L], respectively.

Conclusions: In this large cohort of patients with HoFH, evinacumab was generally well tolerated and markedly decreased LDL-C irrespective of age and sex. Moreover, the efficacy and safety of evinacumab was sustained over the long term.

Citing Articles

Current and Emerging Treatment Options for Hypertriglyceridemia: State-of-the-Art Review.

Zimodro J, Rizzo M, Gouni-Berthold I Pharmaceuticals (Basel). 2025; 18(2).

PMID: 40005962 PMC: 11858358. DOI: 10.3390/ph18020147.


Prioritization of Lipid Metabolism Targets for the Diagnosis and Treatment of Cardiovascular Diseases.

Wang Z, Chen S, Zhang F, Akhmedov S, Weng J, Xu S Research (Wash D C). 2025; 8:0618.

PMID: 39975574 PMC: 11836198. DOI: 10.34133/research.0618.


Homozygous Familial Hypercholesterolemia Treatment: New Developments.

Blom D, Marais A, Raal F Curr Atheroscler Rep. 2025; 27(1):22.

PMID: 39751968 PMC: 11698773. DOI: 10.1007/s11883-024-01269-5.


Management of Hypercholesterolemia in Patients with Coronary Artery Disease: A Glimpse into the Future.

Sciahbasi A, Russo P, Zuccanti M, Chiorazzo L, Castelli F, Granatelli A J Clin Med. 2024; 13(23).

PMID: 39685877 PMC: 11642370. DOI: 10.3390/jcm13237420.


The Biology and Clinical Implications of PCSK7.

Sachan V, Susan-Resiga D, Lam K, Seidah N Endocr Rev. 2024; 46(2):281-299.

PMID: 39661471 PMC: 11894536. DOI: 10.1210/endrev/bnae031.

References
1.
France M, Rees A, Datta D, Thompson G, Capps N, Ferns G . HEART UK statement on the management of homozygous familial hypercholesterolaemia in the United Kingdom. Atherosclerosis. 2016; 255:128-139. DOI: 10.1016/j.atherosclerosis.2016.10.017. View

2.
Orsoni A, Saheb S, Levels J, Dallinga-Thie G, Atassi M, Bittar R . LDL-apheresis depletes apoE-HDL and pre-β1-HDL in familial hypercholesterolemia: relevance to atheroprotection. J Lipid Res. 2011; 52(12):2304-2313. PMC: 3283261. DOI: 10.1194/jlr.P016816. View

3.
Thompson G, Blom D, Marais A, Seed M, Pilcher G, Raal F . Survival in homozygous familial hypercholesterolaemia is determined by the on-treatment level of serum cholesterol. Eur Heart J. 2017; 39(14):1162-1168. DOI: 10.1093/eurheartj/ehx317. View

4.
Belanger A, Akioyamen L, Alothman L, Genest J . Evidence for improved survival with treatment of homozygous familial hypercholesterolemia. Curr Opin Lipidol. 2020; 31(4):176-181. DOI: 10.1097/MOL.0000000000000686. View

5.
Moorjani S, Roy M, Torres A, Betard C, Gagne C, Lambert M . Mutations of low-density-lipoprotein-receptor gene, variation in plasma cholesterol, and expression of coronary heart disease in homozygous familial hypercholesterolaemia. Lancet. 1993; 341(8856):1303-6. DOI: 10.1016/0140-6736(93)90815-x. View