新型替戈拉散口腔崩解片在韩国健康人体内的比较药动学特性评价。

IF 0.9 4区 医学 Q4 PHARMACOLOGY & PHARMACY International journal of clinical pharmacology and therapeutics Pub Date : 2023-09-01 DOI:10.5414/CP204378
Jin A Lee, In Sun Goak, Jiwon Lee, Bongtae Kim, Seol Ju Moon, Yong-Geun Kwak, Min-Gul Kim
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引用次数: 0

摘要

目的:替戈拉赞是一种分化型胃酸泵阻滞剂,属于一类钾竞争型胃酸分泌阻滞剂。为提高患者的服药依从性,研制了替戈拉赞口腔崩解片。本研究的目的是比较50 mg替格拉赞的常规片剂(作为参比药)和ODT(作为试验药)在韩国健康受试者中的药代动力学(PK)和安全性。材料与方法:对48名健康受试者进行开放标签、随机、单剂量、6序列、3期交叉研究。所有受试者均给予单次口服替戈拉赞片剂50mg加水、替戈拉赞50mg加水ODT和替戈拉赞50mg不加水ODT。在给药后48小时内采集连续血液样本。采用LC-MS/MS法测定替戈拉赞及其代谢物M1的血浆浓度,采用非室室法计算药代动力学参数。在整个研究过程中,通过评估不良事件、体格检查、实验室测试结果以及生命体征和心电图测量来评估安全性。结果:共有47名受试者完成了研究。加水的替格拉赞的AUCt、Cmax、AUCinf的几何平均比值的90%置信区间分别为0.8873 ~ 0.9729、0.8865 ~ 1.0569、0.8835 ~ 0.9695;不加水的替格拉赞的AUCt、Cmax、AUCinf的几何平均比值分别为0.9169 ~ 1.0127、0.9569 ~ 1.1276、0.9166 ~ 1.0131。无严重不良事件发生,不良事件均为轻度。结论:加水或不加水的替戈拉赞片与常规片的PK谱相当。在安全性方面没有显著差异。因此,可以不用水服用替戈拉散的新型ODT可能会提高酸相关疾病患者的依从性。
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Evaluation of the comparative pharmacokinetic properties of a new orally disintegrating tablet of tegoprazan in healthy Korean subjects.

Purpose: Tegoprazan is a differentiated gastric acid-pump blocker and belongs to a class of potassium-competitive acid secretion blockers. An orally disintegrating tablet (ODT) of tegoprazan was developed to improve patient compliance. The purpose of this study was to compare pharmacokinetics (PK) and safety profiles between the conventional tablet (as the reference drug) and the ODT (as the test drug) of 50 mg tegoprazan in healthy Korean subjects.

Materials and methods: An open-label, randomized, single-dose, 6-sequence, 3-period crossover study was conducted in 48 healthy subjects. All subjects received a single oral dose of tegoprazan 50 mg tablet with water, tegoprazan 50 mg ODT with water, and tegoprazan 50 mg ODT without water. Serial blood samples were collected up to 48 hours after dosing. Plasma concentrations of tegoprazan and its metabolite M1 were measured by LC-MS/MS, and PK parameters were calculated with a non-compartmental method. Safety was evaluated by means of assessed adverse events, physical examinations, laboratory test results as well as measurements of vital signs and ECG throughout the study.

Results: A total of 47 subjects completed the study. The 90% confidence intervals of the geometric mean ratios for AUCt, Cmax, and AUCinf of tegoprazan were 0.8873 - 0.9729, 0.8865 - 1.0569, and 0.8835 - 0.9695 for the test drug with water to the reference drug and 0.9169 - 1.0127, 0.9569 - 1.1276, and 0.9166 - 1.0131 for the test drug without water to the reference drug, respectively. There were no serious adverse events, and all adverse events were mild.

Conclusion: The PK profiles of tegoprazan were equivalent between the conventional tablet and ODT with or without water. There was no significant difference in the safety profiles. Therefore, the novel ODT of tegoprazan that can be taken without water may improve compliance among patients with acid-related diseases.

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来源期刊
CiteScore
1.70
自引率
12.50%
发文量
116
审稿时长
4-8 weeks
期刊介绍: The International Journal of Clinical Pharmacology and Therapeutics appears monthly and publishes manuscripts containing original material with emphasis on the following topics: Clinical trials, Pharmacoepidemiology - Pharmacovigilance, Pharmacodynamics, Drug disposition and Pharmacokinetics, Quality assurance, Pharmacogenetics, Biotechnological drugs such as cytokines and recombinant antibiotics. Case reports on adverse reactions are also of interest.
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