New pharmacological treatment options for irritable bowel syndrome with constipation

被引:12
作者
Nusrat, Salman [1 ]
Miner, Philip B., Jr. [1 ]
机构
[1] Univ Oklahoma, Sch Med, Dept Med, Sect Digest Dis & Nutr, Oklahoma City, OK 73104 USA
关键词
bile acid transport inhibitor; cholecystokinin receptor antagonist; dexloxiglumide; DSP-6952; elobixibat; guanylate cyclase-C agonist; linaclotide; plecanatide; serotonin agonist; sodium-proton exchange inhibitor; tenapanor; YKP-10811; GUANYLATE-CYCLASE-C; PLACEBO-CONTROLLED TRIAL; ACID TRANSPORTER INHIBITOR; GASTROINTESTINAL-TRACT; ABDOMINAL-PAIN; DOUBLE-BLIND; VISCERAL HYPERSENSITIVITY; CHLORIDE CHANNEL; CCK-1; ANTAGONIST; DRUG DEVELOPMENT;
D O I
10.1517/14728214.2015.1105215
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Constipation predominant irritable bowel syndrome (IBS-C) is a common disorder and accounts for a large number of ambulatory visits. Sensory abnormalities, that is, presence of abdominal pain and discomfort, distinguish IBS-C from chronic idiopathic constipation.Area covered: This review focuses on the pharmacology, efficacy, safety, and future of prucalopride, YKP-10811, DSP-6952, dexloxiglumide, linaclotide, plecanatide, tenapanor, and elobixibat.Expert opinion: It is now well established that treatment focusing only on bowel transit provides incomplete relief to patients with IBS-C. Improved understanding of pathophysiology of IBS-C has led to use of sensory end points like complete spontaneous bowel movements and the FDA combined end point (abdominal pain and complete spontaneous bowel movements) in clinical trials. A number of drugs are in development and provide hope for this challenging group of patients. However, because of recent failures secondary to ineffectiveness and/or adverse events, we cautiously await how clinical data play out in larger studies and in clinical practice.
引用
收藏
页码:625 / 636
页数:12
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