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EU-Förderung (12 Mio. €): Imaging Biomarker (IBs) for Safer Drugs: Validation of Translational Imaging Methods in Drug Safety Assessment - Sofia ref.: 116106 Hor01.01.2017 EU-Rahmenprogramm für Forschung und Innovation "Horizont"

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Imaging Biomarker (IBs) for Safer Drugs: Validation of Translational Imaging Methods in Drug Safety Assessment - Sofia ref.: 116106

1.Our consortium has broad, deep experience of drug development and imaging biomarker (IB) validation. We are internationally recognized experts in transporter biology, animal models of lung injury, toxicology, DCEMRI, compartmental modeling, 1H&129Xe lung MR, and labeling of biologicals with PET and fluorescence tags, together with physicians who care for relevant patients. We have an outstanding record of translating IBs: (a) into animals, (b) into man, (c) into tools which drug developers use with confidence in clinical trials of investigational agents, (d) into regulatory drug development and healthcare. We will develop and validate the required IBs and make them commercially available. 2.Building on our previous work with gadoxetate DCEMRI IBs we will develop and standardise, define sensitivity and specificity in rats, and show valid and comparable data multicentre in human volunteers and patients. 3.We believe the search for IBs of Drug Induced Interstitial Lung Disease (DIILD) should start in DIILD patients. Cancer and rheumatology patients receiving, in their standard care, drugs with DIILD liability, and whose physicians withdraw the drug due to suspected DIILD, will be imaged when symptomatic and followed up. From this we will derive IBs of DIILD which predict outcome. We will also develop IBs from 1H/129Xe MRI and PET to further characterise DIILD, and will back-translate and validate all these IBs in rat models. 4.To better assess biodistribution of biologics, we will thoroughly characterise two well-chosen exemplars in rats, pigs and humans: an antibody biologic and a peptide biologic. We will use 89Zr, 18F and 68Ga PET, fluorescence and MALDI imaging. 5.We will follow an imaging biomarker roadmap to establish (a) that the IBs can be deployed robustly in whatever centre they are needed, (b) the relationship of the IB to underlying biology, (c) how well the IB forecasts clinical outcome, and make appropriate arrangements for dissemination.


Geförderte Unternehmen:

Firmenname Förderungssumme
ABBVIE DEUTSCHLAND GmbH & Co. KG 0,00 €
ACADEMISCH ZIEKENHUIS GRONINGEN 1.010.313 €
Antaros Medical AB 566.025 €
BAYER AG 0,00 €
Bayer Pharma AG 0,00 €
Bioxydyn Ltd. 1.958.392 €
BRUKER BIOSPIN GmbH & Co. KG 0,00 €
BRUKER BIOSPIN MRI GmbH 0,00 €
Centre National de la Recherche Scientifique CNRS 0,00 €
Chalmers Tekniska Hogskola AB 563.003 €
European Organisation for Research AND Treatment OF Cancer Aisbl 414.480 €
GE Healthcare Ltd. 0,00 €
Glaxosmithkline Research & Development Ltd. 0,00 €
Lunds Universitet 721.015 €
Manchester University NHS Foundation Trust 0,00 €
MERCK SHARP & DOHME Corp. 0,00 €
Novo Nordisk A/S 0,00 €
Pfizer Ltd. 0,00 €
SANOFI-AVENTIS DEUTSCHLAND GmbH 0,00 €
Sheffield Teaching Hospitals NHS Foundation Trust 0,00 €
STICHTING AMSTERDAM UMC 75.000 €
STICHTING RADBOUD UNIVERSITAIR MEDISCH CENTRUM 1.310.232 €
STICHTING RADBOUD UNIVERSITEIT 0,00 €
The Leeds Teaching Hospitals National Health Service Trust 0,00 €
The University of Manchester 1.361.021 €
The University of Sheffield 2.077.037 €
Truly Labs AB 1.064.146 €
Universite Bourgogne Europe 250.000 €
University of Leeds 629.336 €

Quelle: https://cordis.europa.eu/project/id/116106

Diese Bekanntmachung wurde von Englisch nach Deutsch übersetzt. Die Bekanntmachung bezieht sich auf einen vergangenen Zeitpunkt, und spiegelt nicht notwendigerweise den heutigen Stand wider.