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特立帕肽:首次批准。

Tenapanor: First Approval.

机构信息

Springer Nature, Private Bag 65901, Mairangi Bay, Auckland, 0754, New Zealand.

出版信息

Drugs. 2019 Nov;79(17):1897-1903. doi: 10.1007/s40265-019-01215-9.

Abstract

The selective sodium hydrogen exchanger 3 (NHE3) inhibitor tenapanor is being developed by Ardelyx Inc. for the treatment of constipation-predominant irritable bowel syndrome (IBS-C) [under the tradename IBSRELA] and for hyperphosphataemia in patients with chronic kidney disease (CKD) on dialysis or with end stage renal disease (ESRD). Based on positive results from the phase III T3MPO trial program, tenapanor was recently approved in the USA for the treatment of IBS-C in adults. This article summarises the milestones in the development of tenapanor leading to this first approval.

摘要

由 Ardelyx Inc. 研发的选择性钠氢交换器 3(NHE3)抑制剂替纳诺尔(商品名:IBSRELA),目前正处于治疗以便秘为主要症状的肠易激综合征(IBS-C)[under the tradename IBSRELA]和治疗接受透析或终末期肾病(ESRD)的慢性肾脏病(CKD)患者高磷血症的 III 期临床试验阶段。基于 III 期 T3MPO 试验项目的阳性结果,替纳诺尔最近在美国获批用于治疗成人 IBS-C。本文总结了替纳诺尔研发过程中的重要里程碑,直至首次获批。

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