针对罕见疾病的药物再利用。

3区 生物学 Q2 Biochemistry, Genetics and Molecular Biology
Juveriya Israr, Shabroz Alam, Ajay Kumar
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引用次数: 0

摘要

针对罕见病的药物再利用是一种具有创造性和成本效益的方法,可为某些疾病提供新的治疗方案。这项技术要求利用有关药理学特征、作用模式、安全性概况以及与生物系统相互作用的既有信息,将现有药物重新用于新用途。由于患者群体小、疾病复杂、对疾病病理生物学了解不足等因素,为不常见疾病开发新的治疗方法往往十分困难。与从零开始开发新药相比,药物再利用是一种更有效、更具成本效益的方法。它通常需要学术界、制药公司和患者权益团体之间的合作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug repurposing for rare diseases.

Repurposing drugs for rare diseases is a creative and cost-efficient method for creating new treatment options for certain conditions. This technique entails repurposing existing pharmaceuticals for new uses by utilizing established information regarding pharmacological characteristics, modes of operation, safety profiles, and interactions with biological systems. Creating new treatments for uncommon diseases is frequently difficult because of factors including small patient groups, disease intricacy, and insufficient knowledge of disease pathobiology. Drug repurposing is a more efficient and cost-effective approach compared to developing new drugs from scratch. It typically requires collaboration among academia, pharmaceutical firms, and patient advocacy groups.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Progress in Molecular Biology and Translational Science (PMBTS) provides in-depth reviews on topics of exceptional scientific importance. If today you read an Article or Letter in Nature or a Research Article or Report in Science reporting findings of exceptional importance, you likely will find comprehensive coverage of that research area in a future PMBTS volume.
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