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| Funder | European Commission |
|---|---|
| Recipient Organization | Universitat Des Saarlandes |
| Country | Germany |
| Start Date | Jun 01, 2022 |
| End Date | Nov 30, 2025 |
| Duration | 1,278 days |
| Number of Grantees | 13 |
| Roles | Participant; Third Party; Coordinator |
| Data Source | European Commission |
| Grant ID | 101057639 |
Polypharmacy, multimorbidity and genetic heterogeneity can affect drug efficacy, raise the risk for adverse drug reactions (ADRs) and increase healthcare costs. ADRs are among the leading causes of death in developed countries and a major cause of hospitalization.
Drug-drug interactions (DDIs) and drug-gene interactions (DGIs) are highly interconnected and require a holistic approach to improve safety of our citizens.
However, investigations on real-life drug-drug-gene interactions (DDGIs) in clinical trials are unfeasible due to combinatorial explosion, high costs and ethical concerns. Hence, significant knowledge gaps exist.
Furthermore, the lack of participation in managing their conditions might be excessively demanding for polymedicated and multimorbid citizens.
SafePolyMed will develop a novel and innovative framework to define, assess and manage DDGIs for physicians and individual patients resulting in education and empowerment of citizens as well as in reduced healthcare costs by improving patient safety.
The main objectives of SafePolyMed are (1) development of a novel, evidence-based risk scoring system using machine learning on large real-world datasets to identify patients at risk; (2) identification and validation of patient reported outcome measures for multifactorial patient safety in collaboration with European patient organizations; (3) development of an electronic tool to empower patients by allowing them to properly manage their therapies, check for and educate about DD(G)Is and collect their patient reported outcomes; (4) mathematical modelling of clinically relevant compounds to derive individualized dose adaptations for safe and effective dose regimens in case of DDGIs, accessible via a web-based decision support system with tailored information for either citizens or physicians and (5) validation of the developed safety tools in a ?proof-of-principle? study including representative patient cohorts from different European clinical sites.
Academisch Ziekenhuis Leiden; Tartu Ulikool; Helsingin Yliopisto; Universitaetsklinikum Aachen; Fraunhofer Gesellschaft Zur Forderung Der Angewandten Forschung Ev; Eurice European Research and Project Office Gmbh; Idryma Technologias Kai Erevnas; Leukanet Ev; Gospodar Zdravja, Spletna Zdravstvena Komunikacija, D.O.O.; Patvocates Gmbh; Panepistimio Patron; Univerza V Ljubljani; Universitat Des Saarlandes
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