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EU-PEARL

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EU Patient cEntric clinicAl tRial pLatform

EU-PEARL has the ambition of transforming the current approach of conducting single-compound clinical trials into the use of cross-company Integrated Research Platforms (IRPs), taking into consideration both patients’ interests an... see more

30/04/2023

FUNDACIO HOSPITAL...

26M€

Project Budget: 26M€

Project leader

FUNDACIO HOSPITAL UNIVERSITARI VALL HEBRON -... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5 | 33M€

PARTICIPATION DEPralty Sin fecha límite de participación.

Ver 38 Participantes

Financing granted El organismo H2020 notifico la concesión del proyecto The day 2023-04-30

IMI2-2018-15-01: Integrated research platforms enabl... Specific Challenge:Despite good progress in many areas of healthcare, it seems that clinical develop...

I+D

Cerrada does 6 years

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characteristics of the participant

Este proyecto no cuenta con búsquedas de partenariado abiertas en este momento.

Private Information

No hay información privada compartida para este proyecto. Habla con el coordinador.

38 Participantes

FUNDACIO HOSPITAL UNIVERSITA...

2.18M€ | Leader

UNISR

734.25K€ | participant

SYNAPSE

97.70K€ | participant

Allergan

N.D. | participant

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Project duration: 41 months Date Start: 2019-11-27
End date: 2023-04-30

Project leader

FUNDACIO HOSPITAL UNIVERSITARI VALL HEBRON -... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5 | 33M€

Project Budget 26M€

participation deadline Sin fecha límite de participación.

Project description EU-PEARL has the ambition of transforming the current approach of conducting single-compound clinical trials into the use of cross-company Integrated Research Platforms (IRPs), taking into consideration both patients’ interests and the opportunities from novel molecules for addressing medical needs. Patient-centric data and knowledge sharing have the potential to accelerate the development of new treatments and reduce the operational costs of clinical trials. EU-PEARL will improve clinical effectiveness, patients’ satisfaction and societal access to timely and affordable medicines and it will shape the clinical trials of the future. This will change the industry paradigm from competition to cooperation in four disease areas and provide the framework for designing IRPs in other disease areas. The main objectives of EU-PEARL are: (1) To create a reusable, accessible and sustainable modular IRP for the design and execution of patient-centric, cross- company IRP in any disease area with unmet needs; (2) To set up the open, dynamic, patient inclusive IRP governance structure that will manage the appropriate regulatory, ethical, legal, statistical and data utilisation requirements of the IRP; (3) To disseminate and exploit the EU-PEARL paradigm through the provision of the necessary common tools, procedures, expertise and operational skills working to the highest scientific, regulatory and ethical standards and best practices, developed jointly by public and industry partners in a consensus-based approach; and (4) To create trial-ready IRP networks in the four disease areas of Major Depressive Disorder (MDD), Tuberculosis (TB), Non-Alcoholic Steatohepatitis (NASH) and Neurofibromatosis (NF).

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