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Saxagliptin: A review of its use as combination therapy in the management of type 2 diabetes mellitus in the EU

机译:沙格列汀:综述其在欧盟2型糖尿病的治疗中的联合治疗

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摘要

Saxagliptin (Onglyza TM) is a dipeptidyl peptidase 4 inhibitor widely approved for the treatment of type 2 diabetes mellitus. In the EU, saxagliptin is indicated as combination therapy with metformin, a sulfonylurea, a thiazolidinedione, or insulin (with or without metformin) for the treatment of adult patients with type 2 diabetes, including those with mild to severe renal impairment. This article reviews the clinical efficacy and tolerability of add-on saxagliptin therapy in patients with type 2 diabetes, in line with its approved indications in the EU, and summarizes the drug's pharmacological properties.The clinical efficacy of saxagliptin 5 mgday in combination with metformin, glibenclamide (glyburide), a thiazolidinedione, or insulin (with or without metformin) has been demonstrated in several randomized, double-blind, placebo-controlled, multicentre, phase III trials (18-104 weeks in duration) in patients with type 2 diabetes. In these trials, glycosylated haemoglobin (HbA 1c) was changed from baseline (primary endpoint) by a greater extent with add-on saxagliptin 5mgday (-1.09% to +0.03%) than with comparator regimens (-0.44% to +0.69%). Two other randomized, double-blind trials showed that saxagliptin 5 mgday as add-on therapy to metformin was noninferior to uptitrated glipizide in terms of lowering HbA1c (-0.74% vs-0.80%) at 52 weeks, or sitagliptin (-0.52% vs-0.62%) at 18 weeks. Saxagliptin 2.5 mgday as add-on to existing anti-diabetic therapy was also effective for up to 52 weeks in a randomized, double-blind, placebo-controlled, multicentre trial in patients with type 2 diabetes and renal impairment (HbA 1c was reduced by 1.08% vs 0.36%; p≤0.007).Saxagliptin as add-on therapy for up to 4 years was generally well tolerated in clinical trials. Treatment with saxagliptin did not increase the risk of hypoglycaemia or cardiovascular outcomes relative to placebo or active comparators, and was generally weight neutral.In conclusion, saxagliptin is a useful option as add-on therapy to metformin, a sulfonylurea, a thiazolidinedione, or insulin (with or without metformin) in patients with type 2 diabetes who require combination therapy.
机译:沙格列汀(Onglyza TM)是一种二肽基肽酶4抑制剂,被广泛批准用于治疗2型糖尿病。在欧盟,沙格列汀被指定为与二甲双胍,磺酰脲,噻唑烷二酮或胰岛素(有或没有二甲双胍)联合治疗成人2型糖尿病患者,包括轻度至重度肾功能不全的患者。本文综述了沙格列汀联合治疗2型糖尿病患者的临床疗效和耐受性,并符合欧盟批准的适应症,并总结了该药的药理特性。沙格列汀5 mgday联合二甲双胍的临床疗效,在2型糖尿病患者的多项随机,双盲,安慰剂对照,多中心,III期试验(持续时间18-104周)中,已证实格列苯脲(格列本脲),噻唑烷二酮或胰岛素(有或没有二甲双胍) 。在这些试验中,添加沙格列汀5mg天(-1.09%至+ 0.03%)的糖基化血红蛋白(HbA 1c)相对于基线(主要终点)的改变程度大于比较者方案(-0.44%至+ 0.69%) 。另外两项随机,双盲试验显示,沙格列汀5 mgday作为二甲双胍的辅助治疗,在52周时降低HbA1c(-0.74%vs-0.80%)或西他列汀(-0.52%vs -0.62%)。在一项随机,双盲,安慰剂对照,多中心试验中,对2型糖尿病和肾功能不全的患者进行的一项随机,双盲,安慰剂对照研究,在现有抗糖尿病药物的基础上加用Saxagliptin 2.5 mgday也可有效长达52周(HbA 1c降低了1.08%对0.36%;p≤0.007)。沙格列汀作为长达4年的附加疗法在临床试验中普遍耐受。相对于安慰剂或活性比较剂,沙格列汀治疗不会增加低血糖或心血管疾病的风险,并且通常是体重中性的。总之,沙格列汀是二甲双胍,磺酰脲类,噻唑烷二酮或胰岛素的附加疗法需要联合治疗的2型糖尿病患者(使用或不使用二甲双胍)。

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