Profiling the toxicity of new drugs a non animal based approach integrating tox...
Profiling the toxicity of new drugs a non animal based approach integrating toxicodynamics and biokinetics
The overall aim of Predict-IV is to develop strategies to improve the assessment of drug safety in the early stage of development and late discovery phase, by an intelligent combination of non animal-based test systems, cell biolo...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
TransQST
Translational quantitative systems toxicology to improve the...
18M€
Cerrado
ONTOX
Ontology driven and artificial intelligence based repeated d...
17M€
Cerrado
DETECTIVE
Detection of endpoints and biomarkers of repeated dose toxic...
9M€
Cerrado
RISK-HUNT3R
RISK assessment of chemicals integrating HUman centric Next...
23M€
Cerrado
NOTOX
Predicting long term toxic effects using computer models bas...
10M€
Cerrado
SCR&TOX
Stem Cells for Relevant Efficient Extended and Normalized To...
9M€
Cerrado
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
The overall aim of Predict-IV is to develop strategies to improve the assessment of drug safety in the early stage of development and late discovery phase, by an intelligent combination of non animal-based test systems, cell biology, mechanistic toxicology and in-silico modelling, in a rapid and cost effective manner. A better prediction of the safety of an investigational compound in early development will be delivered. Margins-of-safety will be deduced and the data generated by the proposed approach may also identify early biomarkers of human toxicity for pharmaceuticals. The results obtained in Predict-IV will enable pharmaceutical companies to create a tailored testing strategy for early drug safety. The project will integrate new developments to improve and optimize cell culture models for toxicity testing and to characterize the dynamics and kinetics of cellular responses to toxic effects in vitro. The target organs most frequently affected by drug toxicity will be taken into account, namely liver and kidney. Moreover, predictive models for neurotoxicty are scarce and will be developed. For each target organ the most appropriate cell model will be used. The approach will be evaluated using a panel of drugs with well described toxicities and kinetics in animals and partly also in humans. This approach will be highly advantageous as it will allow a direct comparison between the in vivo to the in vitro data. A parallel analysis of several dynamic and kinetic models with a broad spectrum of endpoints should allow for the identification of several relevant biomarkers of toxicity. Inter-individual susceptibilities will be taken into account by integrating the polymorphisms of the major drug metabolizing enzymes and correlating the observed effects in the human cell models with their genotype. Environmental influences on cellular toxicity to these compounds will also be evaluated using hypoxic stress as a relevant test model.