Current Approaches to Design Space Development and Regulatory Applications for Drug Products: Findings from the IQ Utilization of Design Space for Filings Working Group Survey.

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY Pharmaceutical Research Pub Date : 2024-09-01 Epub Date: 2024-09-04 DOI:10.1007/s11095-024-03765-4
James E Miesle, Frederick Osei-Yeboah, Anette Pauli-Bruns, Bei Chen, Slobodanka Manceva, Jonathan B Wade, Shawn Yin, Divyakant Desai, Olivier Dirat, Chandan Bhugra, Fanny Stauffer
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Abstract

Purpose: The concept of a Design Space (DSp) was introduced in ICH Q8 as a tool within the quality-by-design (QbD) approach to pharmaceutical development with the intent of being globally applicable. However, there appears to be variance in the regulatory agency expectations in pharmaceutical product filing and implementation of DSp. This paper presents some of the current industry perspective on design space.

Methods: The Utilization of Design Space for Filings (UDSpF) Working Group in the Innovation and Quality (IQ) Consortium conducted a survey to establish a baseline for the current understanding of DSp among IQ member companies and assess the similarities and/or differences in strategies when filing a DSp. The survey focused on how IQ member companies approach DSp development, the primary drivers for the DSp, the presentation of the DSp in the filing, DSp verification and the benefits and flexibility anticipated and/or realized.

Results: A total of 14 responses were received and analyzed representing a small sample size but a large proportion of the innovator industry/large pharmaceutical companies. The survey results revealed that DSp is not yet a commonplace for small molecule drug products and may not even be utilized as much in large molecule drug products. The benefits of DSp, with respect to enhanced process understanding, are well understood by the sponsors; however, the benefits of filed DSp with respect to manufacturing flexibility are not fully realized in the commercial lifecycle of the product. There are also challenges in gaining consistent buy-in/value proposition for DSp among cross-functional teams within organizations.

Conclusions: There are still gaps in design space implementation for its full benefit in the pharmaceutical industry. The WG has presented a unified view from member companies on the approach to DSp considering when/where the DSp experiments are conducted and on the extent of the DSp development proposed in a dossier.

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当前药物产品设计空间开发和监管申请的方法:智商利用设计空间申报工作组调查的结果。
目的:ICH Q8 中引入了设计空间 (DSp) 的概念,将其作为药品开发的质量源于设计 (QbD) 方法中的一种工具,目的是在全球范围内适用。然而,监管机构对医药产品申报和实施 DSp 的期望似乎存在差异。本文介绍了目前业界对设计空间的一些看法:创新与质量 (IQ) 联盟中的申报设计空间利用 (UDSpF) 工作组进行了一项调查,以确定 IQ 成员公司目前对 DSp 的理解基线,并评估申报 DSp 时策略的相似性和/或差异。调查的重点是 IQ 成员公司如何开发 DSp、DSp 的主要驱动因素、DSp 在申报中的表现形式、DSp 验证以及预期和/或实现的效益和灵活性:结果:共收到并分析了 14 份回复,样本量较小,但在创新企业/大型制药公司中占有很大比例。调查结果显示,DSp 在小分子药物产品中尚未普及,甚至在大分子药物产品中也未得到广泛应用。申办者非常了解 DSp 在增强工艺理解方面的益处;但是,在产品的商业生命周期中,申报 DSp 在生产灵活性方面的益处尚未完全实现。此外,在获得组织内跨职能团队对 DSp 的一致认同/价值主张方面也存在挑战:结论:设计空间在制药行业的实施仍存在差距,难以充分发挥其效益。考虑到在何时/何地进行 DSp 实验,以及卷宗中建议的 DSp 开发程度,工作组成员公司就 DSp 方法提出了统一的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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