Decision-Making Criteria and Methods for Initiating Late-Stage Clinical Trials in Drug Development From a Multi-Stakeholder Perspective: A Scoping Review

IF 6.3 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Ce Jiang, Céline Beji, Sonia Zebachi, Ghinwa Y. Hayek, Aysun Cetinyurek-Yavuz, Muhammad Bergas N. Fayyad, Laura Rodwell, Kit C. B. Roes, Billy Amzal, Christoph Gerlinger, Raphaël Porcher, Julien Tanniou
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Abstract

The decision-making process in drug development involves “go/no-go” decisions, particularly at the transition from early to late-stage trials. While the decisions are solely made by drug developers, they must take into account the perspectives of multiple stakeholders—such as regulatory agencies, HTA bodies, payers, patients, and ethics committees—to ensure well-informed and robust decision-making. These perspectives influence key considerations, including resource allocation, risk mitigation, regulatory compliance, etc. To support this process, quantitative methodologies, including Bayesian and hybrid frequentist-Bayesian approaches, have been introduced to improve decision-making. However, these methodologies often do not fully account for the diverse priorities and needs of all stakeholders. This scoping review examines criteria and methods used in decision-making at the phase II to III transition, with a focus on broadening the probability of success (PoS) concept beyond efficacy alone. Our review explores PoS for different success definitions, such as regulatory approval, market access, financial viability, and competitive performance. Key themes include decision criteria selection, trial design optimization, utility-based approaches, financial metrics, and multi-stakeholder considerations in decision-making. Our findings highlight both the limitations of current methodologies and potential paths forward, including the integration of real-world data (RWD) and advanced analytics. This work complements a companion manuscript by Cetinyurek-Yavuz et al. (2025) providing a detailed review of PoS methodologies focused solely on efficacy, specifically PoS for achieving statistical significance in phase III studies, including definitions, terminologies, and analytical approaches. Together, these studies provide a foundation for advancing late-stage trial decisions toward a more balanced, data-driven, and stakeholder-aligned approach.

Abstract Image

多利益相关者视角下药物开发后期临床试验的决策标准和方法:范围综述。
药物开发的决策过程涉及“进行/不进行”的决定,特别是在从早期到后期试验的过渡阶段。虽然决策完全由药物开发商做出,但他们必须考虑多个利益相关者的观点,如监管机构、HTA组织、支付方、患者和伦理委员会,以确保充分了解和健全的决策。这些视角影响关键考虑因素,包括资源分配、风险缓解、法规遵从性等。为了支持这一过程,已经引入了定量方法,包括贝叶斯和混合频率-贝叶斯方法,以改善决策。然而,这些方法往往不能充分考虑所有利益相关者的不同优先事项和需求。这一范围审查审查了在第二阶段到第三阶段过渡期间决策中使用的标准和方法,重点是扩大成功概率(PoS)概念,而不仅仅是功效。我们的回顾探讨了不同成功定义的PoS,如监管批准、市场准入、财务可行性和竞争绩效。关键主题包括决策标准选择、试验设计优化、基于效用的方法、财务指标和决策中的多方利益相关者考虑。我们的研究结果强调了当前方法的局限性和潜在的前进道路,包括现实世界数据(RWD)和高级分析的整合。这项工作补充了Cetinyurek-Yavuz等人(2025)的合著文稿,该文稿详细回顾了仅关注功效的PoS方法,特别是在III期研究中实现统计显著性的PoS,包括定义、术语和分析方法。总之,这些研究为推动后期试验决策朝着更加平衡、数据驱动和利益相关者一致的方向发展奠定了基础。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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