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Funded Projects › HORIZON

ERAMET · Ecosystem for rapid adoption of modelling and simulation METhods to address regulatory needs in the development of orphan and paediatric medicines 

HORIZONStatus: SIGNED1 January 202431 December 2027EU funding €3,865,043Call HORIZON-HLTH-2023-IND-06

ERAMET will provide an integrated approach for developers and regulators’ decision-making for paediatric and orphan drugs, centred on the drug development questions. This will constitute a transparent ecosystem for drug development and assessment, that will facilitate the adoption of modelling and simulation (M&S) methods and related data types (including real word data such as registries and electronic healthcare data).The overall objective of ERAMET is to provide and implement a framework for establishing the credibility of M&S methods and related results as sources of evidence within regulatory procedures.The ecosystem proposed by ERAMET will be based on three pillars: (1) A repository connecting questions, data and methods.(2) The development and validation of high-quality standards for data and analytical methods (including M&S and hybrid approaches). These will cover computational M&S, digital twins, AI, hybrid approaches, standard statistics and pharmacometrics, as analytical methods and alternative data types and sources such as RWD, eHealth data, registries, historical regulatory submissions, scientific and (non)clinical trials). (3) An AI-based platform that will automate and optimise the data collection, formatting and modelling and simulation analysis and implement the credibility assessment. As part of ERAMET, the ecosystem will be applied to five use-cases including paediatric extrapolation and characterisation of drug benefit/risk in 4 groups of rare diseases, namely ataxia, transfusion dependent haemoglobinopathies, bronchopulmonary dysplasia, and paediatric tuberculosis.Each of the use-case is planned to lead to submission and regulatory approval of at least one validated M&S tool via the EMA qualification procedure. Training will be proposed to familiarise regulatory assessors, drug developers and clinical researchers with this new approach.

Consortium · 19 organisations

coordinator

UNIVERSITE DE NAMUR

BE · €1,039,500

participant

UNIVERSITA DEGLI STUDI DI CATANIA

IT · €500,313

associatedPartner

AGENCIA ESPANOLA DE MEDICAMENTOS Y PRODUCTOS SANITARIOS

ES

participant

INE BLANKENBERG SKOTTHEIM RUSTEN

NO

associatedPartner

CERTARA UK LIMITED

UK

participant

ACADEMISCH ZIEKENHUIS GRONINGEN

NL · €345,058

participant

UNIVERSITAT DE VALENCIA

ES · €245,672

participant

ATHINA-EREVNITIKO KENTRO KAINOTOMIAS STIS TECHNOLOGIES TIS PLIROFORIAS, TON EPIKOINONION KAI TIS GNOSIS

EL · €150,000

participant

SYSTEMS RESOURCE LAB AS

NO · €644,565

participant

CONSORZIO PER VALUTAZIONI BIOLOGICHE E FARMACOLOGICHE

IT · €323,879

participant

AGENCE NATIONALE DE SECURITE DU MEDICAMENT ET DES PRODUITS DE SANTE

FR · €100,000

participant

AGENTSCHAP COLLEGE TER BEOORDELING VAN GENEESMIDDELEN

NL · €73,125

thirdParty

FONDAZIONE PER LA RICERCA FARMACOLOGICA GIANNI BENZI ETS

IT

associatedPartner

UNIVERSITY OF WARWICK

UK

associatedPartner

UNIVERSITY COLLEGE LONDON

UK

participant

EUROPEAN BUSINESS SUMMIT NETWORK

BE · €298,745

associatedPartner

ARIDHIA INFORMATICS LIMITED

UK

participant

FEDERAL AGENCY FOR MEDICINES AND HEALTH PRODUCTS

BE · €144,188

participant

APARITO NETHERLANDS BV

NL

Research fields

View the official record on CORDIS →

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