Filippov Sergey, Pinkosky Stephen L, Newton Roger S
Esperion Therapeutics Inc., Ann Arbor, Michigan, USA.
Curr Opin Lipidol. 2014 Aug;25(4):309-15. doi: 10.1097/MOL.0000000000000091.
To review the profile of ETC-1002, as shown in preclinical and clinical studies, including LDL-cholesterol (LDL-C)-lowering activity and beneficial effects on other cardiometabolic risk markers as they relate to the inhibition of adenosine triphosphate-citrate lyase and the activation of adenosine monophosphate-activated protein kinase.
ETC-1002 is an adenosine triphosphate-citrate lyase inhibitor/adenosine monophosphate-activated protein kinase activator currently in Phase 2b clinical development. In seven Phase 1 and Phase 2a clinical studies, ETC-1002 dosed once daily for 2-12 weeks has lowered LDL-C and reduced high-sensitivity C-reactive protein by up to 40%, with neutral to positive effects on glucose levels, blood pressure, and body weight. Importantly, use of ETC-1002 in statin-intolerant patients has shown statin-like lowering of LDL-C without the muscle pain and weakness responsible for discontinuation of statin use by many patients. ETC-1002 has also been shown to produce an incremental benefit, lowering LDL-C as an add-on therapy to a low-dose statin. In over 300 individuals in studies of up to 12 weeks, ETC-1002 has been well tolerated with no serious adverse effects.
Because adenosine triphosphate-citrate lyase and adenosine monophosphate-activated protein kinase play central roles in regulating lipid and glucose metabolism, pharmacological modulation of these two enzymes could provide an important therapeutic alternative for statin-intolerant patients with hypercholesterolemia.
回顾ETC - 1002在临床前和临床研究中的表现,包括其降低低密度脂蛋白胆固醇(LDL - C)的活性以及对其他心血管代谢风险标志物的有益影响,这些影响与抑制三磷酸腺苷 - 柠檬酸裂解酶和激活单磷酸腺苷激活的蛋白激酶有关。
ETC - 1002是一种三磷酸腺苷 - 柠檬酸裂解酶抑制剂/单磷酸腺苷激活的蛋白激酶激活剂,目前正处于2b期临床开发阶段。在7项1期和2a期临床研究中,每日给药一次,持续2 - 12周的ETC - 1002降低了LDL - C,并使高敏C反应蛋白降低了40%,对血糖水平、血压和体重有中性至积极的影响。重要的是,在不耐受他汀类药物的患者中使用ETC - 1002已显示出类似他汀类药物降低LDL - C的效果,而不会出现导致许多患者停用他汀类药物的肌肉疼痛和无力症状。ETC - 1002作为低剂量他汀类药物的附加疗法,也已显示出能进一步降低LDL - C。在长达12周的研究中,超过300名个体对ETC - 1002耐受性良好,无严重不良反应。
由于三磷酸腺苷 - 柠檬酸裂解酶和单磷酸腺苷激活的蛋白激酶在调节脂质和葡萄糖代谢中起核心作用,对这两种酶进行药理调节可为不耐受他汀类药物的高胆固醇血症患者提供重要的治疗选择。