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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.
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页码:181 / 191
页数:11
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