Gatto Nicolle M, Campbell Ulka B
Aetion, Inc., 5 Pennsylvania Plaza, New York, NY, 10001, USA.
Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, USA.
Ther Innov Regul Sci. 2025 Jul 18. doi: 10.1007/s43441-025-00822-x.
Clinical development delays and failures do not serve public health. Reliance solely on expert opinion or historical patterns rather than evidence from representative, real-world point-of-care data about the indication results in suboptimal trial design, missed opportunities, and uninterpretable findings. Investment in real-world evidence (RWE) generation to build a deep, comprehensive, and current understanding of the characteristics, care, and outcomes of the indicated population is essential to improving clinical development decision making. Despite the recognized value of RWE, this evidence generation is not done systematically. Here we make integrated RWE generation more compelling and practicable by addressing concerns we have heard from biopharma leaders and, for emerging RWE leaders, providing a blueprint for designing real-world studies in a phased approach that aligns with clinical development investment. Our work is intended to facilitate more widespread adoption of integrated RWE generation, beginning early in development, so that robust RWE is in hand at the right time for evidence-based decision making by the sponsor, regulators, and payers.
临床开发的延误和失败不利于公众健康。仅依赖专家意见或历史模式,而不是来自关于该适应症的具有代表性的真实世界即时医疗数据的证据,会导致试验设计欠佳、错失机会以及结果难以解读。投入资源生成真实世界证据(RWE),以深入、全面且及时地了解目标人群的特征、治疗情况和结局,对于改善临床开发决策至关重要。尽管RWE的价值已得到认可,但这种证据生成工作并未系统地开展。在此,我们通过回应生物制药行业领导者提出的关切,让整合式RWE生成更具说服力且切实可行,并且为新兴的RWE领导者提供一个蓝图,以便采用分阶段方法设计与临床开发投资相契合的真实世界研究。我们的工作旨在推动整合式RWE生成得到更广泛的应用,从开发早期就开始,以便在合适的时间为申办方、监管机构和支付方提供有力的RWE,用于基于证据的决策。