加速工艺开发和产品配方。

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Pharmaceutical Research Pub Date : 2024-05-01 Epub Date: 2024-05-02 DOI:10.1007/s11095-024-03708-z
Mauricio Futran, Fernando Muzzio, Bikash Chatterjee
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引用次数: 0

摘要

目前,新药上市或批准后变更所需的漫长时间造成了多种问题,如延误患者获得救命或改善生命的新药,以及减缓对需要新疗法的紧急情况的反应速度。然而,新技术的出现有助于解决这些问题。在 2023 年 1 月举行的国家创新和技术促进发展计划(NIPTE)加速药物产品开发和审批寻路研讨会上,与会者审议了产品配方和工艺开发的现状、加速开发时间表的障碍以及利用新技术克服这些障碍的机会。作者参加了这次研讨会,并在本文中分享了他们对一些前进方向的看法,包括先进制造技术和适应性开发。此外,还需要转变监管流程的模式,加强竞争前合作,以及监管机构、行业和学术界之间的共同战略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accelerating Process Development and Product Formulation.

Currently, the lengthy time needed to bring new drugs to market or to implement postapproval changes causes multiple problems, such as delaying patients access to new lifesaving or life-enhancing medications and slowing the response to emergencies that require new treatments. However, new technologies are available that can help solve these problems. The January 2023 NIPTE pathfinding workshop on accelerating drug product development and approval included a session in which participants considered the current state of product formulation and process development, barriers to acceleration of the development timeline, and opportunities for overcoming these barriers using new technologies. The authors participated in this workshop, and in this article have shared their perspective of some of the ways forward, including advanced manufacturing techniques and adaptive development. In addition, there is a need for paradigm shifts in regulatory processes, increased pre-competitive collaboration, and a shared strategy among regulators, industry, and academia.

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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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