重塑治疗性蛋白质:挖掘新疗法的宝藏

Sarfaraz K Niazi, Zamara Mariam
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引用次数: 1

摘要

将批准的治疗蛋白重新用于新剂量、新配方、新给药途径、改进的安全性、新适应症或与药物或放射源的新缀合物,是一种创造性的方法,可以从开发新治疗蛋白的数十亿美元中获益。这些新的机会是最近随着AI/ML工具和高通量筛查技术的出现而创造的。此外,蛋白质的复杂性提供了化学药物所不可能的挖掘机会;在不花费数十亿美元的情况下引入新的疗法,使这条道路在满足人类迫切需求的同时,在经济上非常有利可图。本文分析了几种实用的重新发明方法,并提出了显著降低开发成本的监管策略。这将使数百种新疗法能够以可承受的成本进入市场。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reinventing Therapeutic Proteins: Mining a Treasure of New Therapies
Reinventing approved therapeutic proteins for a new dose, a new formulation, a new route of administration, an improved safety profile, a new indication, or a new conjugate with a drug or a radioactive source is a creative approach to benefit from the billions spent on developing new therapeutic proteins. These new opportunities were created only recently with the arrival of AI/ML tools and high throughput screening technologies. Furthermore, the complex nature of proteins offers mining opportunities that are not possible with chemical drugs; bringing in newer therapies without spending billions makes this path highly lucrative financially while serving the dire needs of humanity. This paper analyzes several practical reinventing approaches and suggests regulatory strategies to reduce development costs significantly. This should enable the entry of hundreds of new therapies at affordable costs.
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