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Engineering of a GLP-1 analogue peptide/anti-PCSK9 antibody fusion for type 2 diabetes treatment

机译:用于2型糖尿病治疗的GLP-1类似物肽/抗PCSK9抗体融合的工程设计

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摘要

Type 2 diabetes (T2D) is a complex and progressive disease requiring polypharmacy to manage hyperglycaemia and cardiovascular risk factors. However, most patients do not achieve combined treatment goals. To address this therapeutic gap, we have developed MEDI4166, a novel glucagon-like peptide-1 (GLP-1) receptor agonist peptide fused to a proprotein convertase subtilisin/kexin type 9 (PCSK9) neutralising antibody that allows for glycaemic control and low-density lipoprotein cholesterol (LDL-C) lowering in a single molecule. The fusion has been engineered to deliver sustained peptide activity in vivo in combination with reduced potency, to manage GLP-1 driven adverse effects at high dose, and a favourable manufacturability profile. MEDI4166 showed robust and sustained LDL-C lowering in cynomolgus monkeys and exhibited the anticipated GLP-1 effects in T2D mouse models. We believe MEDI4166 is a novel molecule combining long acting agonist peptide and neutralising antibody activities to deliver a unique pharmacology profile for the management of T2D.
机译:2型糖尿病(T2D)是一种复杂且进行性疾病,需要多药店来管理高血糖症和心血管危险因素。但是,大多数患者没有达到综合治疗目标。为了解决这一治疗空白,我们开发了MEDI4166,这是一种新型的胰高血糖素样肽1(GLP-1)受体激动剂肽,与前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型(PCSK9)中和抗体融合,可实现血糖控制和低血糖。降低单个分子中的密度脂蛋白胆固醇(LDL-C)。该融合蛋白经过改造,可在体内提供持续的肽活性,同时降低了药效,可在高剂量下处理GLP-1驱动的不良反应,并具有良好的可制造性。 MEDI4166在食蟹猴中显示出强大且持续的LDL-C降低,并在T2D小鼠模型中表现出预期的GLP-1作用。我们相信,MEDI4166是结合长效激动剂肽和中和抗体活性的新型分子,可为T2D的治疗提供独特的药理学特征。

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