Icosabutate for the treatment of very high triglycerides: A placebo-controlled, randomized, double-blind, 12-week clinical trial

被引:18
|
作者
Bays, Harold E. [1 ]
Hallen, Jonas [2 ]
Vige, Runar [2 ]
Fraser, David [2 ]
Zhou, Rong [3 ]
Hustvedt, Svein Olaf [2 ]
Orloff, David G. [3 ]
Kastelein, John J. P. [4 ]
机构
[1] L MARC Res Ctr, Louisville, KY USA
[2] Pronova BioPharma, Lysaker, Norway
[3] Medpace Inc, Cincinnati, OH USA
[4] Univ Amsterdam, Acad Med Ctr, Dept Vasc Med, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
关键词
Hypertriglyceridemia; Icosabutate; Triglycerides; Apolipoprotein C-III; Remnants; APOLIPOPROTEIN C-III; ENHANCED FATTY-ACID; CARDIOVASCULAR-DISEASE; DENSITY-LIPOPROTEIN; RISK; ASSOCIATION; CHOLESTEROL; HYPERTRIGLYCERIDEMIA; OMEGA-3-FATTY-ACIDS; DYSLIPIDEMIA;
D O I
10.1016/j.jacl.2015.10.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
BACKGROUND: Icosabutate is a structurally enhanced omega-3 fatty acid molecule developed with the aim of achieving improved triglyceride (TG)-lowering efficacy, increased potency, and preserved safety compared with conventional prescription omega-3 fatty acid. OBJECTIVE: To evaluate the efficacy and safety of icosabutate 600 mg once daily in patients with very high TGs. METHODS: After a 6-8 week run-in period, men and women with TG levels >= 500 mg/dL and <= 1500 mg/dL were randomized to double-blind treatment with placebo or icosabutate 600 mg for 12 weeks. The primary end point was % change from baseline in TGs at 12 weeks. RESULTS: A total of 87 subjects were randomized. At baseline, median TG (interquartile range) levels were 611 (543-878) and 688 (596-892) mg/dL, and the median change after 12 weeks of treatment was -51% and -17%, respectively, for a placebo-corrected change of -33% (P < .001). Adjusted for placebo, icosabutate significantly reduced very low-density lipoprotein cholesterol (-36%, P < .001), remnant lipoprotein cholesterol (-34%, P < .001), apolipoprotein (Apo) C-III (-35%, P < .001), trended toward reduced non-high-density lipoprotein cholesterol (-7%, P = .064); significantly increased high-density lipoprotein cholesterol (18%, P < .001) and low density lipoprotein cholesterol (28%, P < .001), with a trend of an increased lipoprotein (a; 10%, P = .054). No changes were observed in total cholesterol, apolipoprotein B, or apolipoprotein Al. Fasting plasma glucose was unchanged, whereas fasting plasma insulin was reduced (P = .001) with icosabutate. Icosabutate was generally well tolerated. CONCLUSION: Treatment with icosabutate once daily significantly reduced TG, very low-density lipoprotein cholesterol, and Apo C-III levels in patients with very high TG levels. This trial was registered at www.clinicaltrials.gov as NCT01893515. (C) 2016 National Lipid Association. All rights reserved.
引用
收藏
页码:181 / 191
页数:11
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