Tack Jan, Vladimirov Borislav, Horny Ivo, Chong Chui Fung, Eisner Jessica, Czerniak Richard, Takanami Yohei
Department of Gastroenterology, University Hospitals Leuven, Leuven, Belgium.
Department of Gastroenterology, University Hospital "Queen Giovanna- ISUL", Medical University of Sofia, Sofia, Bulgaria.
Neurogastroenterol Motil. 2023 Jan;35(1):e14468. doi: 10.1111/nmo.14468. Epub 2022 Sep 30.
Proton-pump inhibitors (PPIs) are cornerstone treatments for gastro-esophageal reflux disease (GERD); however, evidence suggests that most patients exhibit partial response to PPIs, suggesting the need for novel therapies that can provide an improved and sustained increase in gastric pH.
This study aimed to determine the effect of vonoprazan, a novel, orally active small-molecule potassium-competitive acid blocker, versus esomeprazole, a PPI, in preventing heartburn symptoms over a 4-week treatment period in patients with GERD and a partial response to esomeprazole treatment.
This randomized, double-blind, proof-of-concept, phase 2 clinical trial was conducted between 2016 and 2018 at 39 sites across Europe and designed to evaluate the efficacy and safety of vonoprazan 20 mg once daily (q.d.) and 40 mg q.d. versus esomeprazole 40 mg q.d. after 1:1:1 randomization of symptomatic patients with GERD and a partial response to a healing dose of esomeprazole.
Overall, 256 eligible patients (female, 59.4%; mean age, 52.6 years) received vonoprazan 20 mg (n = 85), vonoprazan 40 mg (n = 85), or esomeprazole 40 mg (n = 86); mean (SD) percentages of heartburn-free 24-h periods during double-blind treatment were 36.7% (33.4%), 36.5% (35.6%), and 38.4% (34.8%), respectively, with no intergroup statistical significance. Vonoprazan exposure increased proportionally from the 20-mg to 40-mg dose (mean C : 23.3 ng/ml to 47.1 ng/ml, respectively). Most treatment-emergent adverse events were mild, with no deaths reported.
No statistically significant difference in efficacy and safety was observed among treatment groups, and vonoprazan was well tolerated. The trial is registered with the National Board of Health (EudraCT: 2015-001154-14) database.
质子泵抑制剂(PPIs)是胃食管反流病(GERD)的基础治疗药物;然而,有证据表明大多数患者对PPIs仅表现出部分反应,这表明需要新的疗法来提高并持续提升胃内pH值。
本研究旨在比较新型口服活性小分子钾竞争性酸阻滞剂沃克(vonoprazan)与质子泵抑制剂埃索美拉唑在GERD患者中预防烧心症状的效果,这些患者对埃索美拉唑治疗有部分反应,治疗周期为4周。
这项随机、双盲、概念验证的2期临床试验于2016年至2018年在欧洲的39个地点进行,旨在评估沃克20毫克每日一次(q.d.)和40毫克q.d.与埃索美拉唑40毫克q.d.的疗效和安全性,将有症状且对埃索美拉唑愈合剂量有部分反应的GERD患者按1:1:1随机分组。
总体而言,256名符合条件的患者(女性占59.4%;平均年龄52.6岁)接受了20毫克沃克(n = 85)、40毫克沃克(n = 85)或40毫克埃索美拉唑(n = 86)治疗;双盲治疗期间无烧心24小时周期的平均(标准差)百分比分别为36.7%(33.4%)、36.5%(35.6%)和38.4%(34.8%),组间无统计学差异。沃克的暴露量从20毫克剂量到40毫克剂量成比例增加(平均Cmax:分别从23.3纳克/毫升增加到47.1纳克/毫升)。大多数治疗中出现的不良事件为轻度,无死亡报告。
各治疗组在疗效和安全性方面未观察到统计学显著差异,沃克耐受性良好。该试验已在国家卫生委员会(EudraCT:2015 - 001154 - 14)数据库注册。