Current state-of-the-art and gaps in platform trials: 10 things you should know, insights from EU-PEARL

Other authors

Institut Català de la Salut

[Koenig F] Medical University of Vienna, Center for Medical Data Science, Vienna, Austria. [Spiertz C] Janssen Biologics BV, Leiden, the Netherlands. [Millar D] Former Employee, Janssen Research & Development, LLC, Raritan, NJ, USA. [Rodríguez-Navarro S] Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. [Machín N] TEAM-IT Research S.L., Barcelona, Spain. [Van Dessel A] Janssen Pharmaceutica NV, Beerse, Belgium. [Genescà J, Pericàs JM] Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Spanish Network of Biomedical Research Centers, Digestive and Liver Diseases (CIBERehd), Madrid, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-02-12T12:14:19Z

2024-02-12T12:14:19Z

2024-01



Abstract

Adaptive designs; Clinical research; Patient-centred


Diseños adaptativos; Investigación clínica; Centrada en el paciente


Dissenys adaptatius; Recerca clínica; Centrada en el pacient


Platform trials bring the promise of making clinical research more efficient and more patient centric. While their use has become more widespread, including their prominent role during the COVID-19 pandemic response, broader adoption of platform trials has been limited by the lack of experience and tools to navigate the critical upfront planning required to launch such collaborative studies. The European Union-Patient-cEntric clinicAl tRial pLatform (EU-PEARL) initiative has produced new methodologies to expand the use of platform trials with an overarching infrastructure and services embedded into Integrated Research Platforms (IRPs), in collaboration with patient representatives and through consultation with U.S. Food and Drug Administration and European Medicines Agency stakeholders. In this narrative review, we discuss the outlook for platform trials in Europe, including challenges related to infrastructure, design, adaptations, data sharing and regulation. Documents derived from the EU-PEARL project, alongside a literature search including PubMed and relevant grey literature (e.g., guidance from regulatory agencies and health technology agencies) were used as sources for a multi-stage collaborative process through which the 10 more important points based on lessons drawn from the EU-PEARL project were developed and summarised as guidance for the setup of platform trials. We conclude that early involvement of critical stakeholder such as regulatory agencies or patients are critical steps in the implementation and later acceptance of platform trials. Addressing these gaps will be critical for attaining the full potential of platform trials for patients.


EU-PEARL has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 853966. This Joint Undertaking receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA.

Document Type

Article


Published version

Language

English

Publisher

Elsevier

Related items

eClinicalMedicine;67

https://doi.org/10.1016/j.eclinm.2023.102384

info:eu-repo/grantAgreement/EC/H2020/847989

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Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

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