Phase I Study to Evaluate the Effect of Hepatic Impairment on Pharmacokinetics and Safety of Tegoprazan, a Potassium Competitive Acid Blocker

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Anhye Kim, Dongseong Shin, Youlim Seo, Deborah Kang, Yang Won Min, In Hee Kim, Jungryul Kim
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Abstract

Introduction

Tegoprazan is a potassium-competitive acid blocker, and its systemic exposure is presumably affected by hepatic clearance and bioavailability. This study aimed to investigate the effect of hepatic impairment (HI) on the safety and pharmacokinetics of tegoprazan and metabolite.

Methods

An open-label, multicenter, parallel-group study was conducted in patients with mild (n = 8), moderate (n = 8) and severe (n = 1) HI according to the Child–Pugh classification as well as controls. Healthy subjects (n = 8) were matched to patients with the moderate category based on age, body mass index and sex. Blood and urine samples were obtained to evaluate the concentrations of tegoprazan and metabolite (M1) until 48 h after a single oral administration of 50 mg of tegoprazan.

Results

The geometric mean ratio with a 90% confidence interval of maximum plasma concentration and area under the plasma concentration–time curve for tegoprazan in patients with impaired hepatic function compared to controls were 0.8228 (0.4997–1.3550) and 1.2264 (0.7447–2.0197) in the mild category, 1.0332 (0.6274–1.7015) and 1.7676 (1.0733–2.9109) in the moderate category, and 1.0699 (0.3713–3.0823) and 1.9567 (0.6792–5.6377) in the severe category. The half-life, apparent clearance, renal clearance, and fraction unbound to plasma protein were comparable across study groups. The plasma concentration of M1 increased and decreased faster in the normal group. Tegoprazan was generally well tolerated in patients with HI.

Conclusions

Systemic exposure to tegoprazan tended to be increased in subjects with HI. The difference between patients with mild HI and the controls was deemed not to require dose adjustment for tegoprazan.

Clinical Trial Registration

ClinicalTrials.gov identifiers: NCT04494269 (31 Jul 2020).

Abstract Image

评估肝功能损害对钾竞争酸阻滞剂替戈拉赞药代动力学和安全性影响的I期研究。
替戈拉赞是一种钾竞争性酸阻滞剂,其全身暴露可能受到肝脏清除和生物利用度的影响。本研究旨在探讨肝功能损害(HI)对替格拉赞及其代谢物的安全性和药代动力学的影响。方法:采用开放标签、多中心、平行组研究方法,根据Child-Pugh分级对轻度(n = 8)、中度(n = 8)和重度(n = 1) HI患者及对照组进行研究。健康受试者(n = 8)根据年龄、体重指数和性别与中度患者配对。在单次口服替戈拉赞50mg后48小时,采集血液和尿液样本以评估替戈拉赞及其代谢物(M1)的浓度。结果:几何平均比率的90%置信区间最大血浆浓度和血浆浓度时间曲线下的面积tegoprazan肝脏功能受损患者相比,控制分别为0.8228(0.4997 - -1.3550)和1.2264(0.7447 - -2.0197)温和的类别,1.0332(0.6274 - -1.7015)和1.7676(1.0733 - -2.9109)温和的类别,和1.0699(0.3713 - -3.0823)和1.9567(0.6792 - -5.6377)在严重的类别。半衰期、表观清除率、肾脏清除率和未与血浆蛋白结合的比例在各研究组之间具有可比性。正常组血浆M1浓度升高和降低较快。替戈拉赞在HI患者中耐受性良好。结论:HI患者对替戈拉散的全身暴露倾向于增加。轻度HI患者与对照组之间的差异被认为不需要调整替戈拉赞的剂量。临床试验注册:ClinicalTrials.gov标识符:NCT04494269(2020年7月31日)。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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