米氮平和替扎尼定在新原料药Dorsumio®中的联合药代动力学参数、安全性和药物-药物相互作用

A. Goncharov, A. Grigoriev, A. Globenko, I. Goncharov, K. A. Muratov, D. V. Yaroshenko, A. Sidorova, A. Kapashin, O. Kovchan, A. I. Bashkatova, M. Pasko
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引用次数: 0

摘要

目的:研究健康志愿者一次服用Dorsumio®(米氮平+替扎尼定缓释片,15 mg + 6 mg,俄罗斯JSC Valenta Pharm)的药代动力学参数及安全性,并与单组分药物Calixta®(INN:米氮平,薄膜片,30 mg,克罗地亚共和国Belupo, Drugs and Cosmetics d.d.d .)和Sirdalud®MR (INN:米氮平+替扎尼定缓释片,15 mg + 6 mg)进行比较。替扎尼定,缓释胶囊,6毫克,诺华制药股份公司,瑞士)与他们的药物相互作用的评价时,同时或单独服用。材料和方法。对复方药物Dorsumio®的药代动力学和安全性进行了一项两阶段、随机、比较交叉研究。在第一阶段,志愿者在两个给药周期内轮流服用一片或两片研究药物;在第二阶段,受试者在三个给药期交替服用参考单药Calixta®和Sirdalud®MR和联合用药。共有38名志愿者被随机纳入研究,其中14人参加了第一阶段的研究,24人参加了第二阶段的研究。采用高效液相色谱-串联质谱法测定米氮平和替扎尼定的定量水平。根据所得数据,计算出反映每种药物生物利用度的主要药代动力学参数,并研究其联合用药对药代动力学的相互影响。在研究过程中监测受试者的生命体征和实验室参数,记录不良事件(ae)和严重ae的发生情况。联合用药Dorsumio®剂量增加两倍,导致单个药物的药代动力学相应增加。米氮平和替扎尼定对其药代动力学参数没有明显的相互作用。在参与第二阶段研究的一名受试者中,在联合使用Calixta®和Sirdalud®MR后,记录了两个轻微的副作用,不需要医疗干预,并自行解决,没有健康后果。米氮平和替扎尼定以自由或固定组合的形式联合使用的安全性没有差异。结果表明,所研究的药物组合对单个成分的药代动力学没有相互影响。
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Pharmacokinetic parameters, safety and drug-drug interactions of mirtazapine and tizanidine, combined in the new original drug Dorsumio®
Objective: to study the pharmacokinetic parameters and safety of Dorsumio® (mirtazapine + tizanidine, extended-release tablets, 15 mg + 6 mg, JSC Valenta Pharm, Russia) taken once by healthy volunteers in comparison with Calixta®, a monocomponent drug (INN: Mirtazapine, filmcoated tablets, 30 mg, Belupo, Drugs and Cosmetics d.d., Republic of Croatia) and Sirdalud® MR (INN: Tizanidine, modified-release capsules, 6 mg, Novartis Pharma AG, Switzerland) with an evaluation of their drug interactions when taken concomitantly or separately.Material and methods. A two-stage, randomized, comparative cross-over study of the pharmacokinetics and safety of the complex drug Dorsumio® was conducted. In the first stage, volunteers alternated between taking one or two tablets of the study drug in two administration periods; in the second stage, subjects alternated between taking the reference monodrugs Calixta® and Sirdalud® MR alone and in a joint combination in three administration periods. A total of 38 volunteers were randomized into the study, of which 14 subjects participated in the first and 24 in the second stage of the study. Quantitative levels of mirtazapine and tizanidine were determined by high-performance liquid chromatography with tandem mass spectrometry. Based on the data obtained, the main pharmacokinetic parameters reflecting the bioavailability of each drug were calculated, and the mutual influence of their combination on pharmacokinetics was also studied. During the study, vital signs and laboratory parameters of the subjects were monitored, and the occurrence of adverse events (AEs) and serious AEs was recorded.Results. A two-fold increase in the dose of the combination drug Dorsumio® resulted in a comparable increase in the pharmacokinetics of the individual drugs. There was no significant reciprocal effect of mirtazapine and tizanidine on their pharmacokinetic parameters. In one of the subjects participating in the second stage of the study, two mild side effects were registered after the joint use of Calixta® and Sirdalud® MR that did not require medical intervention and resolved on their own without health consequences.Conclusion. There were no differences in the safety profile of the combined use of mirtazapine and tizanidine in the form of a free or fixed combination. It was shown that the investigated drug combination had no mutual influence on the pharmacokinetics of the individual components.
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