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摘要
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Pemafibrate (Parmodia (R)) is a novel, highly selective peroxisome proliferator-activated receptor (PPAR)-alpha modulator (SPPARM). It acts by binding to PPAR-alpha and regulating the expression of target genes that modulate lipid metabolism, thereby decreasing plasma triglyceride levels and increasing high-density lipoprotein cholesterol levels. Developed by Kowa Company, Ltd., oral pemafibrate has been approved in Japan for the treatment of hyperlipidaemia (including familial hyperlipidaemia). This article summarizes the milestones in the development of pemafibrate leading to this first global approval for hyperlipidaemia.
Keyword:
PPAR-ALPHA MODULATOR
SPPARM-ALPHA
DYSLIPIDEMIC PATIENTS
DOUBLE-BLIND
K-877
HYPERLIPIDEMIA
POTENT
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引用论文
The novel selective PPARα modulator (SPPARMα) pemafibrate improves dyslipidemia, enhances reverse cholesterol transport and decreases inflammation and atherosclerosis
ATHEROSCLEROSIS
IF5.7
Effects of K-877, a novel selective PPARα modulator (SPPARMα), in dyslipidaemic patients: A randomized, double blind, active- and placebo-controlled, phase 2 trial
ATHEROSCLEROSIS
IF5.7
Selective peroxisome proliferator-activated receptor-α modulator K-877 efficiently activates the peroxisome proliferator-activated receptor-α pathway and improves lipid metabolism in mice选择性过氧化物酶体增殖物激活受体-α 调节剂K-877有效激活过氧化物酶体增殖物激活受体-α 途径并改善小鼠脂质代谢
Efficacy and safety of K-877, a novel selective peroxisome proliferator-activated receptor α modulator (SPPARMα), in combination with statin treatment: Two randomised, double-blind, placebo-controlled clinical trials in patients with dyslipidaemia
ATHEROSCLEROSIS
IF5.7
Effects of K-877, a novel selective PPARα modulator, on small intestine contribute to the amelioration of hyperlipidemia in low-density lipoprotein receptor knockout mice新型选择性ppar α 调节剂K-877对小肠的影响有助于改善低密度脂蛋白受体基因敲除小鼠的高脂血症
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