Division of Pharmacoepidemiology and Clinical Pharmacology, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, Utrecht, The Netherlands.
Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.
Clin Pharmacol Ther. 2022 Aug;112(2):344-352. doi: 10.1002/cpt.2628. Epub 2022 May 17.
Decentralized clinical trials (DCTs) have the potential to improve accessibility, diversity, and retention in clinical trials by moving trial activities to participants' homes and local surroundings. In this study, we conducted semi-structured interviews with 20 European regulators to identify regulatory challenges and opportunities for the implementation of DCTs in the European Union. The key opportunities for DCTs that were recognized by regulators include a reduced participation burden, which could facilitate the participation of underserved patients. In addition, regulators indicated that data collected in DCTs are expected to be more representative of the real world. Key challenges recognized by regulators for DCTs include concerns regarding investigator oversight and participants' safety when physical examinations and face-to-face contact are limited. To facilitate future learning, hybrid clinical trials with both on-site and decentralized elements are proposed by the respondents.
去中心化临床试验 (DCTs) 有可能通过将试验活动转移到参与者的家庭和当地环境中,提高临床试验的可及性、多样性和保留率。在这项研究中,我们对 20 名欧洲监管机构进行了半结构化访谈,以确定在欧盟实施 DCT 的监管挑战和机遇。监管机构认可的 DCT 的主要机会包括减轻参与负担,这可以促进服务不足的患者的参与。此外,监管机构表示,DCT 中收集的数据预计更能代表真实世界。监管机构认为 DCT 的主要挑战包括当身体检查和面对面接触受到限制时,对研究者监督和参与者安全的担忧。为了促进未来的学习,受访者提出了具有现场和去中心化元素的混合临床试验。