首页> 外文期刊>International journal of clinical practice >Long-term safety and efficacy of linagliptin as monotherapy or in combination with other oral glucose-lowering agents in 2121 subjects with type 2 diabetes: Up to 2 years exposure in 24-week phase III trials followed by a 78-week open-label extension
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Long-term safety and efficacy of linagliptin as monotherapy or in combination with other oral glucose-lowering agents in 2121 subjects with type 2 diabetes: Up to 2 years exposure in 24-week phase III trials followed by a 78-week open-label extension

机译:利格列汀作为单一疗法或与其他口服降糖药联用在2121位2型糖尿病患者中的长期安全性和有效性:在24周的III期临床试验中暴露2年,然后进行78周的开放标签延长

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Aim: The aim of this study was to evaluate the long-term safety, tolerability and efficacy of the dipeptidyl peptidase-4 inhibitor linagliptin given either alone or in combination with other oral glucose-lowering agents in persons with type 2 diabetes. Methods: A 78-week open-label extension study evaluated subjects who participated in one of four preceding 24-week, randomised, double-blind, placebo-controlled parent trials and who received linagliptin, linagliptin + metformin, linagliptin + metformin + a sulphonylurea or linagliptin + pioglitazone (all with linagliptin administered orally once daily). Individuals receiving one of these treatments during a previous trial continued the same treatment (n = 1532) for up to a total of 102 weeks, whereas those previously receiving placebo were switched to linagliptin (n = 589). All 2121 participants received at least one dose of the trial medication and were included in the primary safety analysis. Results: In subjects previously receiving active treatment, the glycosylated haemoglobin A 1c reduction achieved during the 24-week parent trials was sustained through the 78-week extension period (change from baseline to week 102: -0.8%). Drug-related adverse events were experienced by 14.3% of participants. Hypoglycaemia occurred in 13.9% of participants and was similar between those previously receiving treatment (13.6%) and those switching from placebo to linagliptin (14.6%). Hypoglycaemia occurred most frequently with the use of metformin + a sulphonylurea background therapy (11%). Overall, no clinically relevant changes in body weight were observed. Conclusion: Long-term treatment with linagliptin was well tolerated with no change in the safety profile observed during the extension study. Sustained long-term glycaemic control was maintained for up to 102 weeks with either linagliptin monotherapy or linagliptin in combination with other oral glucose-lowering agents.
机译:目的:本研究旨在评估二肽基肽酶-4抑制剂利格列汀在2型糖尿病患者中单独或与其他口服降糖药联合使用的长期安全性,耐受性和疗效。方法:一项为期78周的开放标签扩展研究评估了参加过之前四个为期24周,随机,双盲,安慰剂对照的父母试验之一的受试者,并接受了利格列汀,利格列汀+二甲双胍,利格列汀+二甲双胍+磺脲类药物或利格列汀+吡格列酮(均与利格列汀每天口服一次)。在先前的试验中接受这些治疗方法之一的患者继续进行相同的治疗(n = 1532),总共长达102周,而先前接受安慰剂的患者则改用linagliptin(n = 589)。所有2121名参与者均接受了至少一剂试验药物,并被纳入主要安全性分析。结果:在先前接受积极治疗的受试者中,在24周的父母试验期间达到的糖基化血红蛋白A 1c降低持续了78周(从基线到102周的变化:-0.8%)。 14.3%的参与者经历了与药物相关的不良事件。低血糖发生在13.9%的参与者中,与先前接受治疗的参与者(13.6%)和从安慰剂改为利格列汀的参与者(14.6%)相似。低血糖症最常发生于使用二甲双胍+磺酰脲类背景疗法(11%)。总体而言,未观察到体重的临床相关变化。结论:利拉列汀的长期治疗耐受性良好,在扩展研究期间未观察到安全性变化。利格列汀单一疗法或利格列汀与其他口服降糖药联合使用可维持长达102周的长期血糖控制。

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