Lee Seong-Wook, Jeon You Hyun, Lim Jeong-Hoon, Seo Jung Ju, Jung Hee-Yeon, Choi Ji-Young, Park Sun-Hee, Kim Chan-Duck, Kim Yong-Lim, Cho Jang-Hee
Division of Nephrology, Department of Internal Medicine, School of Medicine, Kyungpook National University Hospital, Kyungpook National University, Daegu 41944, Republic of Korea.
Pharmaceuticals (Basel). 2025 Jun 1;18(6):830. doi: 10.3390/ph18060830.
: Potassium-competitive acid blockers (P-CABs) offer rapid gastric acid inhibition and lower toxicity compared to proton pump inhibitors (PPIs). This study investigates the drug-drug interaction between P-CABs and immunosuppressants tacrolimus and mycophenolate in kidney transplant recipients (KTRs). : Sixty-two KTRs were randomized to receive either 50 mg of tegoprazan or 20 mg of pantoprazole. Patients were monitored using a smart clinical trial platform incorporating remote monitoring and safety management systems, which tracked drug adherence and vital signs. General and gastrointestinal (GI) symptoms were surveyed via a self-developed app on patients' phones. Trough levels of tacrolimus and mycophenolate were measured every 4 weeks over 12 weeks. : Medication adherence was 100% in both groups. A total of 13,726 biometric data points and 5031 questionnaire responses were collected, with 5704 feedback messages and 56 video visits conducted. At 12 weeks, the mean trough levels of tacrolimus and mycophenolate were similar between the tegoprazan and pantoprazole groups (5.5 ± 1.6 vs. 5.8 ± 2.0 ng/mL, = 0.50 and 2.7 ± 1.4 vs. 2.6 ± 1.4 µg/mL, = 0.57, respectively). The intragroup difference in trough levels from baseline to week 12 was not significant in either group. GI symptoms scores, vital signs, and allograft function remained stable and comparable between groups. : Tegoprazan does not alter the blood trough levels of tacrolimus and mycophenolate during the 12-week follow-up in KTRs and has a similar impact on GI symptoms as pantoprazole. This study confirms the feasibility and safety of using a smart clinical trial system with remote monitoring for randomized trials.
钾离子竞争性酸阻滞剂(P-CABs)与质子泵抑制剂(PPIs)相比,能更快地抑制胃酸分泌,且毒性更低。本研究调查了P-CABs与免疫抑制剂他克莫司和霉酚酸酯在肾移植受者(KTRs)中的药物相互作用。62名KTRs被随机分为两组,分别接受50毫克替戈拉赞或20毫克泮托拉唑治疗。使用一个整合了远程监测和安全管理系统的智能临床试验平台对患者进行监测,该平台可跟踪药物依从性和生命体征。通过患者手机上的一个自行开发的应用程序对一般症状和胃肠道(GI)症状进行调查。在12周内,每4周测量一次他克莫司和霉酚酸酯的谷浓度。两组的药物依从性均为100%。共收集了13726个生物特征数据点和5031份问卷回复,进行了5704次反馈消息和56次视频问诊。在12周时,替戈拉赞组和泮托拉唑组他克莫司和霉酚酸酯的平均谷浓度相似(分别为5.5±1.6对5.8±2.0纳克/毫升,P=0.50;2.7±1.4对2.6±1.4微克/毫升,P=0.57)。两组从基线到第12周谷浓度的组内差异均无统计学意义。两组间的胃肠道症状评分、生命体征和移植肾功能均保持稳定且相当。在KTRs的12周随访期间,替戈拉赞不会改变他克莫司和霉酚酸酯的血药谷浓度,且对胃肠道症状的影响与泮托拉唑相似。本研究证实了使用带有远程监测的智能临床试验系统进行随机试验的可行性和安全性。