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Dalcetrapib, a cholesteryl ester transfer protein modulator

机译:Dalcetrapib,胆固醇酯转移蛋白调节剂

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Introduction: Cholesteryl ester transfer protein (CETP) plays an important role in reverse cholesterol transport by transferring cholesteryl esters from high-density lipoprotein (HDL) to the apolipoprotein B-containing lipoproteins. Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis. Dalcetrapib is an orally administered CETP inhibitor developed for the treatment of primary hypercholesterolaemia and mixed hyperlipidaemia. Areas covered: Areas covered are: mode of action, preclinical development and clinical trials of dalcetrapib, a CETP modulator. The article provides an understanding of the pharmacokinetic and pharmacodynamic characteristics of dalcetrapib and insight into its clinical efficacy and safety. In clinical trials, dalcetrapib produced significant elevations in HDL-cholesterol when taken alone or in combination with statin with no effect on blood pressure or expression of genes involved in the reninangiotensinaldosterone system. Expert opinion: Although dalcetrapib is the least potent CETP inhibitor, it does not impair the formation of CETP-induced pre-β HDL, which might be needed to increase reverse cholesterol transport. While dalcetrapib is well-tolerated and does not show major side effects, the recent interim results of the Phase III dal-OUTCOMES trial have shown the lack of a clinically meaningful benefit, and further testing of the drug has been halted.
机译:简介:胆固醇酯转移蛋白(CETP)通过将胆固醇酯从高密度脂蛋白(HDL)转移到含载脂蛋白B的脂蛋白,在胆固醇逆向转运中发挥重要作用。抑制CETP是增加HDL-胆固醇并可能减少动脉粥样硬化的目标。 Dalcetrapib是一种口服CETP抑制剂,被开发用于治疗原发性高胆固醇血症和混合性高脂血症。涵盖的领域:涵盖的领域是:CETP调节剂dalcetrapib的作用方式,临床前开发和临床试验。这篇文章提供了对达塞曲匹的药代动力学和药效学特性的了解,并深入了解了其临床疗效和安全性。在临床试验中,达塞曲匹单独或与他汀类药物合用时,HDL-胆固醇显着升高,而对血压或肾血管紧张素-醛固酮系统相关基因的表达没有影响。专家意见:尽管dalcetrapib是最无效的CETP抑制剂,但它不会损害CETP诱导的前βHDL的形成,这可能是增加逆向胆固醇转运所必需的。尽管达塞曲匹耐受性好且未显示主要副作用,但最近进行的dal-OUTCOMES III期临床试验的中期结果显示,其缺乏临床意义的益处,并且已停止对该药物的进一步测试。

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