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| Funder | European Commission |
|---|---|
| Recipient Organization | Sigmund Freud Privatuniversitat Wien Gmbh |
| Country | Austria |
| Start Date | Jan 01, 2025 |
| End Date | Dec 31, 2029 |
| Duration | 1,825 days |
| Number of Grantees | 52 |
| Roles | Associated Partner; Participant; Third Party; Coordinator |
| Data Source | European Commission |
| Grant ID | 101165912 |
RealiseD implements a collaborative and compRehensive mEthodological and operational Approach to cLinical trIalS in rarE Diseasesenabling timely drug development and approval centred on patients’ needs with high level of evidence reachable in a limitedenvironment.
The core of RealiseD operational approaches includes the systematic procedures for patients’ referral, the certification ofclinical sites and filling the gaps for successful development of rare and ultra rare diseases[(U)RD]’ clinical trials using 4 (U)RD diseasesfrom 4 European Research Networks (ERNs).
RealiseD methodological teams will optimise innovative statistical and quantitativeapproaches for design and analysis of (U)RD-CTs developed in the past 10-years and refined in the last years to facilitate the regulatorypathway for innovative drug development.
RealiseD is implemented in a public private partnership consortium including regulatorsand HTA bodies representatives to co-create operational and methodological approaches in an iterative procedure using amultistakeholders’ agreement process.
RealiseD will increase the incentives and motivation for the pharmaceutical industry byreducing many uncertainties on the path of drug development in (U)RD that will follow widely accepted rules.
To achieve theseinnovative approaches, RealiseD will capitalise on an international multistakeholders effort as the problem in (U)RD drugdevelopment cannot be solved in a restricted geographical area.
With the development and deployment of playbooks arising from theco-created developments, RealiseD will ascertain visibility and readiness of the innovations.
The overall ambition of RealiseD is tochange the paradigm of CT design for U(RD) by enlarging the spectrum of methodological and operational approaches and toestablish a sustainable, innovative, and optimised CT paradigm for U(RD) medicinal product development programs, whilemaximizing the acceptance by all stakeholders.
Bayer Public Limited Company; Alexion Pharmaceuticals Inc; Universiteit Hasselt; Medizinische Universitaet Wien; Eatris Eric; Humanitas University; Astrazeneca Uk Limited; Fundacio Privada Per A la Recerca I la Docencia Sant Joan de Deu; Institut National de la Sante Et de la Recherche Medicale; Sanofi-Aventis Deutschland Gmbh; Sanofi Winthrop Industrie; Ucb Biopharma; Otto-Von-Guericke-Universitaet Magdeburg; Janssen Research & Development, Llc; Universiteit Gent; Sanofi Srl; Sanofi Genzyme; Eurordis - Rare Diseases Europe; Novartis Pharma Ag; Assistance Publique Hopitaux de Paris; Ipsen Innovation Sas; Istituto Ortopedico Rizzoli; Servier Bio-Innovation Llc; Conect4Children Stichting; Sanofi-Aventis Belgium Sa; Stiftung Fur Qualitat Und Wirtschaftlichkeit Im Gesundheitswesen; F. Hoffmann-la Roche Ag; Genzyme Argentinia S.A.; Stichting Radboud Universitair Medisch Centrum; Hospital Sant Joan de Deu; Paris-Lodron-Universitat Salzburg; Sigmund Freud Privatuniversitat Wien Gmbh; Boehringer Ingelheim Pharma Gmbh &Co Kg; Ruhr-Universitaet Bochum; Boehringer Ingelheim Internationalgmbh; Teamit Research Sl; Universitetet I Oslo; Universitatsklinikum Heidelberg; International Drug Development Institute Sa; Bayer Aktiengesellschaft; Critical Path Institute Stichting; Sanofi-Aventis Recherche & Developpement; Sanofi Aventis Sa; Sanofi; Novo Nordisk A/S; Institut de Recherches Internationales Servier; Universitaetsmedizin Goettingen - Georg-August-Universitaet Goettingen - Stiftung Oeffentlichen Rechts; Fundacio Hospital Universitari Vall D'Hebron - Institut de Recerca; Hopitaux Universitaires de Strasbourg; The European Medicines Agency; Azienda Sanitaria Universitaria Friuli Centrale; Janssen Pharmaceutica Nv
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