Pharmacokinetics and Pharmacodynamics of a Fixed-Dose Combination of Esomeprazole and Magnesium Hydroxide Compared to the Enteric-Coated Esomeprazole.

IF 3.2 4区 医学 Q2 PHARMACOLOGY & PHARMACY Clinical therapeutics Pub Date : 2024-09-16 DOI:10.1016/j.clinthera.2024.08.006
Yoonjin Kim, Sungyeun Bae, Inseung Jeon, Jihoon Kwon, Sung Hee Hong, Na Young Kim, Kyung-Sang Yu, In-Jin Jang, SeungHwan Lee
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Abstract

Purpose: A fixed-dose combination (FDC) of proton pump inhibitors (PPIs) and antacid salts enables rapid acid suppression through the neutralizing effect of the antacid salt and the rapid absorption of PPIs. This study aimed to compare the pharmacokinetics (PKs) and pharmacodynamics (PDs) of a recently formulated FDC of esomeprazole and magnesium hydroxide to the enteric-coated esomeprazole in healthy subjects.

Methods: A randomized, open-label, multiple-dose, two-treatment, two-way crossover design was conducted in healthy subjects. Forty-nine subjects were randomized to one of the two treatment sequences and received either the test drug (esomeprazole/magnesium hydroxide 40/350 mg) or reference drug (enteric-coated esomeprazole 40 mg) for 7 days in the first period and the alternative in the second period with a 14-day washout period. Blood samples were collected for up to 24 hours for PK assessment, and 24-hour gastric pH monitoring was conducted for PD assessment both before and after a single administration, as well as at a steady state after seven consecutive days of administration. The PK and PD parameters were compared between the two drugs.

Findings: After multiple administrations, the median value of time to reach maximum concentration was faster in the test drug than in the reference drug, with a difference of 1.68 hours. The overall systemic exposure of the test drug was similar to that of the reference drug, and the PK parameter fell within the equivalence criteria. The test drug demonstrated a shorter time to reach gastric pH ≥ 4 compared to the reference drug (P = 0.0463). A decrease from baseline in integrated gastric acidity over 24 hours, which represents the degree of inhibition of gastric acid secretion, was equivalent between the two drugs.

Implications: The fixed-dose combination of esomeprazole and magnesium hydroxide showed rapid absorption and quicker gastric acid suppression than enteric-coated esomeprazole with comparable PK and PD properties.

Clinicaltrials: gov identifier: NCT04324905 (https://classic.

Clinicaltrials: gov/ct2/show/NCT04324905).

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埃索美拉唑和氢氧化镁固定剂量复方制剂的药代动力学和药效学与肠溶埃索美拉唑的比较。
目的:质子泵抑制剂(PPIs)和抗酸盐的固定剂量复方制剂(FDC)可通过抗酸盐的中和作用和 PPIs 的快速吸收实现快速抑酸。本研究旨在比较最近配制的埃索美拉唑和氢氧化镁 FDC 与肠溶埃索美拉唑在健康受试者中的药代动力学(PKs)和药效学(PDs):在健康受试者中进行了随机、开放标签、多剂量、两种治疗、双向交叉设计。49名受试者被随机分配到两种治疗顺序中的一种,在第一阶段接受试验药物(埃索美拉唑/氢氧化镁 40/350 毫克)或参照药物(肠溶埃索美拉唑 40 毫克)治疗 7 天,在第二阶段接受另一种药物治疗,并有 14 天的冲洗期。在单次给药前和给药后,以及在连续给药七天后的稳定状态下,均采集长达 24 小时的血样进行 PK 评估,并进行 24 小时胃 pH 监测以评估 PD。对两种药物的 PK 和 PD 参数进行了比较:多次给药后,试验药达到最大浓度的时间中值比参照药快,相差 1.68 小时。试验药物的总体全身暴露量与参比药物相似,PK 参数符合等效标准。与参比药物相比,试验药物达到胃 pH ≥ 4 的时间更短(P = 0.0463)。24小时内综合胃酸度从基线开始下降的幅度(代表胃酸分泌的抑制程度)与两种药物相当:意义:埃索美拉唑和氢氧化镁的固定剂量复方制剂与肠溶型埃索美拉唑相比,吸收更快,胃酸抑制更快,PK 和 PD 特性相当:NCT04324905(https://classic.Clinicaltrials: gov/ct2/show/NCT04324905)。
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来源期刊
Clinical therapeutics
Clinical therapeutics 医学-药学
CiteScore
6.00
自引率
3.10%
发文量
154
审稿时长
9 weeks
期刊介绍: Clinical Therapeutics provides peer-reviewed, rapid publication of recent developments in drug and other therapies as well as in diagnostics, pharmacoeconomics, health policy, treatment outcomes, and innovations in drug and biologics research. In addition Clinical Therapeutics features updates on specific topics collated by expert Topic Editors. Clinical Therapeutics is read by a large international audience of scientists and clinicians in a variety of research, academic, and clinical practice settings. Articles are indexed by all major biomedical abstracting databases.
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