Suppr超能文献

西格玛-2受体的变构拮抗剂——埃莱塔(CT1812)作为轻度至中度阿尔茨海默病的治疗候选药物:一项范围界定性系统评价

The Allosteric Antagonist of the Sigma-2 Receptors-Elayta (CT1812) as a Therapeutic Candidate for Mild to Moderate Alzheimer's Disease: A Scoping Systematic Review.

作者信息

Rasheed Anum, Zaheer Ahmad Bin, Munawwar Aqsa, Sarfraz Zouina, Sarfraz Azza, Robles-Velasco Karla, Cherrez-Ojeda Ivan

机构信息

Department of Research, Services Institute of Medical Sciences, Lahore 54000, Pakistan.

Department of Research, Al Nafees Medical College and Hospital, Isra University, Islamabad 44000, Pakistan.

出版信息

Life (Basel). 2022 Dec 20;13(1):1. doi: 10.3390/life13010001.

Abstract

Nearly 35 million people worldwide live with Alzheimer's disease (AD). The prevalence of the disease is expected to rise two-fold by 2050. With only symptomatic treatment options available, it is essential to understand the developments and existing evidence that aims to target brain pathology and dementia outcomes. This scoping systematic review aimed to collate existing evidence of CT1812 for use in patients with AD and summarize the methodologies of ongoing trials. Adhering to PRISMA Statement 2020 guidelines, PubMed/MEDLINE, Embase, Cochrane, and ClinicalTrials.gov were systematically searched through up to 15 November 2022 by applying the following keywords: CT1812, Alzheimer's disease, dementia, and/or sigma-2 receptor. Three completed clinical trials were included along with three ongoing records of clinical trials. The three completed trials were in Phases I and II of testing. The sample size across all three trials was 135. CT1812 reached endpoints across the trials and obtained a maximum concentration in the cerebrospinal fluid with 97-98% receptor occupancy. The findings of this systematic review must be used with caution as the results, while mostly favorable so far, must be replicated in higher-powered, placebo-controlled Phase II-III trials.

摘要

全球近3500万人患有阿尔茨海默病(AD)。预计到2050年,该病的患病率将增加一倍。由于目前只有对症治疗方案,因此了解旨在针对脑部病变和痴呆症结局的研究进展和现有证据至关重要。本范围界定性系统评价旨在整理CT1812用于AD患者的现有证据,并总结正在进行的试验的方法。遵循《2020年PRISMA声明》指南,截至2022年11月15日,通过应用以下关键词对PubMed/MEDLINE、Embase、Cochrane和ClinicalTrials.gov进行了系统检索:CT1812、阿尔茨海默病、痴呆症和/或σ-2受体。纳入了三项已完成的临床试验以及三项正在进行的临床试验记录。三项已完成的试验处于I期和II期测试阶段。所有三项试验的样本量为135。CT1812在各项试验中均达到终点,在脑脊液中达到最大浓度,受体占有率为97%-98%。本系统评价的结果必须谨慎使用,因为尽管目前的结果大多有利,但仍需在更高效能、安慰剂对照的II-III期试验中进行重复验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d48/9866790/c543a6645f48/life-13-00001-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验