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Gliclazide modified release.

机译:格列齐特修饰释放。

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摘要

Gliclazide modified release (MR) is a new formulation of the drug gliclazide and is given once daily. The hydrophilic matrix of hypromellose-based polymer in the new formulation effects a progressive release of the drug which parallels the 24-hour glycaemic profile in untreated patients with type 2 diabetes mellitus. The formulation shows high bioavailability and its absorption profile is unaffected by coadministration with food. Mean plasma glucose levels are significantly reduced over a 24-hour period in patients with type 2 diabetes mellitus treated with gliclazide MR once daily, in both fasting and postprandial states. No cardiovascular ATP-sensitive potassium channel interaction has been observed at therapeutic concentrations of gliclazide MR. Gliclazide MR has also demonstrated antioxidant properties that are independent of glycaemic control. In a randomised, double-blind, multicentre study, gliclazide MR 30 to 120 mg once daily showed similar efficacy to gliclazide immediate release (IR) 80 to 320 mg/day (in divided doses for doses >80 mg) in patients with type 2 diabetes mellitus over a 10-month period, reducing glycosylated haemoglobin (HbA(1c)) and fasting plasma glucose (FPG) to a similar extent. The drug appeared most efficacious in patients who had previously been treated by diet alone, where significant reductions in HbA(1c) from baseline of 0.9% and 0.95% were seen at 10 and 24 months. Similarly, a sustained effect of gliclazide MR was observed in a subgroup of elderly patients defined a priori; HbA(1c) was decreased to a similar degree to that observed in the general study population. Gliclazide MR showed similar tolerability to gliclazide IR after 10 months' treatment in the randomised trial. The most commonly observed adverse events were arthralgia, arthritis, back pain and bronchitis (each <5%). Bodyweight remained stable. In this study no episodes of nocturnal hypoglycaemia or hypoglycaemia requiring third party assistance were observed during treatment with gliclazide MR. Episodes of symptomatic hypoglycaemia were infrequent, occurring in approximately 5% of patients.
机译:格列齐特缓释(MR)是格列齐特药物的新配方,每天给药一次。在新配方中,基于羟丙甲纤维素的聚合物的亲水性基质可实现药物的逐步释放,这与未经治疗的2型糖尿病患者的24小时血糖曲线相似。该制剂显示出高的生物利用度,并且其吸收特性不受与食物合用的影响。在禁食和餐后状态下,每天两次使用格列齐特MR治疗的2型糖尿病患者,平均血糖水平在24小时内显着降低。在治疗浓度的格列齐特MR中未观察到心血管ATP敏感性钾通道相互作用。格列齐特MR还已证明其抗氧化特性与血糖控制无关。在一项随机,双盲,多中心研究中,对于2型患者,格列齐特MR 30至120 mg每日一次显示与格列齐特立即释放(IR)80至320 mg /天(分剂量> 80 mg)相似的疗效糖尿病在10个月内减少糖基化血红蛋白(HbA(1c))和空腹血糖(FPG)达到相似程度。该药物在以前仅通过饮食治疗的患者中似乎最有效,在10个月和24个月时,HbA(1c)从基线显着降低0.9%和0.95%。同样,在先验定义的老年患者亚组中观察到了格列齐特MR的持续作用。 HbA(1c)降低的程度与一般研究人群中观察到的相似。在随机试验中,格列齐特MR治疗10个月后显示出与格列齐特IR相似的耐受性。最常见的不良事件是关节痛,关节炎,背痛和支气管炎(每个<5%)。体重保持稳定。在这项研究中,格列齐特MR治疗期间未观察到夜间低血糖发作或需要第三方协助的低血糖发作。有症状的低血糖发作很少见,约有5%的患者发生。

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