Catholic Photomedicine Research Institute, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Department of Internal Medicine, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, Goyang, South Korea.
Aliment Pharmacol Ther. 2023 Jan;57(1):72-80. doi: 10.1111/apt.17255. Epub 2022 Oct 31.
Tegoprazan is a novel potassium-competitive acid blocker used to treat acid-related disorders.
To compare tegoprazan 25 mg with lansoprazole 15 mg as maintenance therapy in healed erosive oesophagitis (EE) METHODS: In this phase 3, double-blind, multi-centre study, patients with endoscopically confirmed healed EE were randomised 1:1 to receive tegoprazan 25 mg or lansoprazole 15 mg once daily for up to 24 weeks. The primary efficacy endpoint was the endoscopic remission rate after 24 weeks. The secondary efficacy endpoint was the endoscopic remission rate after 12 weeks. Safety endpoints included adverse events, clinical laboratory results and serum gastrin and pepsinogen I/II levels.
We randomised patients to tegoprazan 25 mg (n = 174) or lansoprazole 15 mg (n = 177). Most had mild EE (Los Angeles (LA) grade A: 57.3%, LA grade B: 37.3%). The endoscopic remission rate after 24 weeks was 90.6% with tegoprazan and 89.5% with lansoprazole. Tegoprazan was not inferior to lansoprazole for maintaining endoscopic remission at 24 weeks and 12 weeks. In subgroup analysis, tegoprazan 25 mg showed no significant difference in maintenance rate according to LA grade (p = 0.47). The maintenance effect of tegoprazan was consistent in CYP2C19 extensive metabolisers (p = 0.76). Increases in serum gastrin were not higher in tegoprazan-treated than lansoprazole-treated patients.
Tegoprazan 25 mg was non-inferior to lansoprazole 15 mg in maintenance of healing of mild EE. In this study, tegoprazan had a similar safety profile to lansoprazole.
替戈拉赞是一种新型钾竞争性酸阻滞剂,用于治疗与酸相关的疾病。
比较替戈拉赞 25mg 与兰索拉唑 15mg 作为愈合性食管炎(EE)的维持治疗。
在这项 3 期、双盲、多中心研究中,内镜证实愈合性 EE 的患者按 1:1 随机分配,接受替戈拉赞 25mg 或兰索拉唑 15mg 每日 1 次,最长 24 周。主要疗效终点为 24 周后的内镜缓解率。次要疗效终点为 12 周后的内镜缓解率。安全性终点包括不良事件、临床实验室结果以及血清胃泌素和胃蛋白酶原 I/II 水平。
我们将患者随机分配至替戈拉赞 25mg(n=174)或兰索拉唑 15mg(n=177)组。大多数患者为轻度 EE(洛杉矶(LA)分级 A:57.3%,LA 分级 B:37.3%)。替戈拉赞 24 周后的内镜缓解率为 90.6%,兰索拉唑为 89.5%。替戈拉赞在 24 周和 12 周时维持内镜缓解方面不劣于兰索拉唑。亚组分析显示,替戈拉赞 25mg 按 LA 分级维持率无显著差异(p=0.47)。替戈拉赞在 CYP2C19 广泛代谢者中的维持效果一致(p=0.76)。替戈拉赞治疗组的血清胃泌素升高并不高于兰索拉唑治疗组。
替戈拉赞 25mg 在维持轻度 EE 的愈合方面不劣于兰索拉唑 15mg。在这项研究中,替戈拉赞的安全性与兰索拉唑相似。