Experimental drugs for erosive esophagitis: what is in the clinical development pipeline?

被引:0
作者
Simadibrata, Daniel Martin [1 ,2 ,3 ]
Lesmana, Elvira [2 ,3 ]
Lee, Yeong Yeh [4 ,5 ]
机构
[1] Case Western Reserve Univ, Metrohlth Med Ctr, Dept Med, Cleveland, OH USA
[2] Univ Indonesia, Med, Jakarta, Indonesia
[3] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[4] Univ Sains Malaysia, Sch Med Sci, Kota Baharu, Malaysia
[5] Hosp USM, GI Funct & Motil Unit, Kota Baharu, Malaysia
关键词
Erosive esophagitis; mucosal protectants; prokinetics; TLESR reducers; proton pump inhibitors; potassium-competitive acid blockers; GASTROESOPHAGEAL-REFLUX DISEASE; PROTON PUMP INHIBITOR; COMPETITIVE ACID BLOCKER; DOUBLE-BLIND; SPHINCTER RELAXATIONS; ARBACLOFEN PLACARBIL; COMBINATION THERAPY; PLUS MOSAPRIDE; GERD PATIENTS; EFFICACY;
D O I
10.1080/13543784.2024.2393868
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionProton pump inhibitor (PPI) has revolutionized the treatment of erosive esophagitis (EE) in the past few decades. However, roughly 30-40% of the patients, especially those with severe EE (Los Angeles Grade C/D), remain poorly responsive to this medication. Novel drugs have been formulated and/or repurposed to address this problem.Areas coveredThis review highlights novel drugs that have been investigated for use in EE, such as mucosal protectants, prokinetics, transient lower esophageal sphincter relaxation (TLESR) reducers, novel PPIs, and the new potassium-competitive acid blocker (PCAB). Studies have demonstrated that PCAB has promising results (efficacy and safety) compared to PPI for the healing of EE, especially in severe diseases.Expert opinionPCAB has gained interest in recent years, with pharmacokinetics and pharmacodynamics properties surpassing PPI. Although recent data on PCABs, which comprised mainly of Vonoprazan, have shown promising results, more randomized controlled trials for other PCAB drugs are needed to elucidate and confirm the superiority of this drug class to PPI, the current first-line treatment of EE.
引用
收藏
页码:1009 / 1018
页数:10
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