Needs assessment for creation of a platform trial network in metabolic-dysfunction associated steatohepatitis

Other authors

Institut Català de la Salut

[Sena E, Muñoz-Martínez S, Rivera-Esteban J, Jiménez-Masip A, Martínez-Gómez M, Genescà J, Pericàs JM] Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Spanish Network of Biomedical Research on Digestive and Liver Diseases (CIBERehd), Barcelona, Spain. [Tacke F] Department of Hepatology and Gastroenterology, Charité - Universitätsmedizin Berlin, Berlin, Germany. [Anstee QM] Liver Unit, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK. Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK. [Di Prospero N] Janssen Research and Development, Raritan, NJ, USA. [Skalshøi- Kjær M] Novo Nordisk A/S, Bagsvaerd, Denmark

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-09-16T05:44:54Z

2024-09-16T05:44:54Z

2024-07-16



Abstract

Trial network; Steatohepatitis; Metabolic-dysfunction


Red de ensayos; Esteatohepatitis; Disfunción metabólica


Xarxa d'assaigs; Esteatohepatitis; Disfunció metabòlica


Background The EU Patient-cEntric clinicAl tRial pLatforms (EU-PEARL) project (IMI2-853966) aimed to develop tools to establish integrated research platforms (IRP) for conducting adaptive-design trials in various diseases, including metabolic-dysfunction associated steatohepatitis (MASH). One essential component of a successful MASH IRP is a robust and reliable Clinical Research Network (CRN). Herein, we outline the required elements and anticipated steps to set-up such a CRN. Methods We identified European clinical research sites that could potentially serve as the foundation for MASH IRP and a CRN. A survey was sent to sites to assess their interest in joining a CRN, their familiarity with platform trials, and their capacity to participate in a future MASH IRP. Results A total of 141 investigators were invited to participate in the survey, and 40% responded. More than half of the answers (52%) identify MASH with advanced fibrosis (F3-4) as the subpopulation with the greatest unmet need. Regarding the difficulty in identifying candidates for trials, 65% find it is moderately difficult and 30% very difficult. Most respondents (94%) believe that a platform trial could offer substantial benefits to patients. Nearly all researchers express interest in participating in a platform trial (78%), with 22% indicating their interest would be contingent on initial industry funding. Conclusion While preliminary, our findings on responding sites are encouraging for the potential establishment of a CRN for a MASH IRP. However, funding schemes and sustainability strategies to provide proof-of-platform in MASH seem key in the short-term scenario.

Document Type

Article


Published version

Language

English

Publisher

Springer Nature

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Attribution 4.0 International

http://creativecommons.org/licenses/by/4.0/

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