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评价普卡那肽治疗 65 岁及以上慢性特发性便秘和便秘型肠易激综合征患者的疗效。

Evaluation of Plecanatide for the Treatment of Chronic Idiopathic Constipation and Irritable Bowel Syndrome With Constipation in Patients 65 Years or Older.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA; Veterans Affairs Ann Arbor Healthcare System, Ann Arbor, MI, USA.

Salix Pharmaceuticals Inc., Bridgewater, NJ, USA.

出版信息

Clin Ther. 2020 Jul;42(7):1406-1414.e4. doi: 10.1016/j.clinthera.2020.05.012. Epub 2020 Jul 10.

Abstract

PURPOSE

Chronic idiopathic constipation (CIC) and irritable bowel syndrome with constipation (IBS-C) are common functional gastrointestinal disorders. The prevalence of constipation-related issues tends to increase with age. This analysis pooled data from Phase III trials in CIC and IBS-C to assess the safety and efficacy of plecanatide in patients aged ≥65 years.

METHODS

Patients randomized to receive plecanatide (3 or 6 mg) or placebo from two CIC and two IBS-C trials were pooled. Efficacy end points common to all trials included changes in stool consistency (Bristol Stool Form Scale), changes in weekly frequency of complete spontaneous bowel movements (CSBMs) and spontaneous bowel movements (SBMs), and time to first CSBM and SBM. Efficacy and safety profile results are reported per age group (≥65 and <65 years of age).

FINDINGS

The pooled intention-to-treat population comprised 451 patients aged ≥65 years (mean age, 70 years) and 4364 patients aged <65 years (mean age, 41.9 years), of whom 287 and 2914, respectively, were randomized to receive plecanatide. Compared with placebo, plecanatide produced statistically significant improvements in stool consistency from baseline at week 12 (both age groups), CSBM and SBM frequency from baseline at week 12 (plecanatide 3 mg group aged ≥65 years and both plecanatide groups aged <65 years), and time from start of therapy to first CSBM (both age groups) and SBM (plecanatide 6 mg group aged ≥65 years and both plecanatide groups aged <65 years). No new safety issues were observed.

IMPLICATIONS

Plecanatide is a well-tolerated and effective treatment option for patients aged ≥65 years with CIC or IBS-C. CLINICALTRIALS.

GOV IDENTIFIERS

NCT01982240, NCT02122471, NCT02387359, and NCT02493452.

摘要

目的

慢性特发性便秘(CIC)和便秘型肠易激综合征(IBS-C)是常见的功能性胃肠疾病。便秘相关问题的患病率往往随年龄增长而增加。本分析汇总了 CIC 和 IBS-C 三项 III 期临床试验的数据,以评估普卡那肽在 65 岁及以上患者中的安全性和疗效。

方法

将来自两项 CIC 和两项 IBS-C 试验中随机接受普卡那肽(3 或 6mg)或安慰剂的患者进行汇总。所有试验共有的疗效终点包括粪便稠度的变化(布里斯托粪便形态量表)、每周完全自发性排便次数(CSBMs)和自发性排便次数(SBMs)的变化,以及首次 CSBM 和 SBM 的时间。按年龄组(≥65 岁和<65 岁)报告疗效和安全性概况结果。

结果

汇总的意向治疗人群包括 451 名≥65 岁的患者(平均年龄 70 岁)和 4364 名<65 岁的患者(平均年龄 41.9 岁),其中分别有 287 名和 2914 名随机接受普卡那肽治疗。与安慰剂相比,普卡那肽在第 12 周时从基线开始显著改善粪便稠度(两个年龄组),在第 12 周时从基线开始显著改善 CSBM 和 SBM 频率(≥65 岁的普卡那肽 3mg 组和所有<65 岁的普卡那肽组),并从治疗开始到首次 CSBM(两个年龄组)和 SBM(≥65 岁的普卡那肽 6mg 组和所有<65 岁的普卡那肽组)的时间。未观察到新的安全性问题。

结论

普卡那肽是一种耐受性良好且有效的治疗选择,可用于治疗≥65 岁的 CIC 或 IBS-C 患者。临床试验。

政府标识符

NCT01982240、NCT02122471、NCT02387359 和 NCT02493452。

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