CIT Joins EUR 10 Million R&D Project Funded By EU and European Cosmetic Industry
Published: Jan 13, 2011
CIT is one of 14 industrial and academic partners in the project, which is coordinated by Inserm, the French National Institute for Health and Medical Research. The “ScreenTox” project will be funded as part of a research cluster with an overall budget of EUR 50 million. This cluster covers seven projects and represents a unique joint effort from the European Commission and the European Cosmetic Association (COLIPA).
In the development of products for use by humans, it is vital to identify compounds with toxic properties at an early stage of their development, in order to avoid spending time and resources on unsuitable and potentially unsafe candidate products. Human pluripotent stem cells offer an unparalleled opportunity to create a wide variety of human cell-based test systems because these cells may be expanded indefinitely and triggered to differentiate into any cell type. The “ScreenTox” project aims at making use of these two attributes in order to optimize current processes and develop novel methods to achieve functional differentiation of human-based target cells in vitro.
The project recognizes a major paradigm shift in predictive toxicology that pluripotent stem cells will permit in the coming years. “The evaluation of toxicants calls for new models that will allow assessing toxicity pathway responses in vitro,” said Marc Peschanski, a leading scientist in the field of toxicity and coordinator of the network. “Derivatives of pluripotent stem cell lines are likely to be the best candidates to implement this new strategy, as these most relevant and reliable model systems can also be robust and scalable in order to meet the challenges of industrial-scale screens.”
"ScreenTox has the potential to generate a huge leap forward in toxicity testing as it combines three key factors: a wide range of international scientific expertise and industry know-how as well as substantial financial investment,” said Roy Forster, CIT's scientific director. “We believe that ScreenTox will demonstrate advantages in using stem cells to assess how safe new products will be for use on humans, and in refining, reducing or even replacing the use of animals for testing.”
About CIT http://www.citox.com
CIT is a science-driven, independent, non-clinical contract research organization (CRO) specialized in safety and health research. Founded in 1969, CIT has carried out a vast number of projects for international companies on human and veterinary pharmaceuticals, biotechnology, chemicals, agrochemicals and consumer products. It has contributed to many product registrations around the world.
With a staff of 350, CIT offers a full range of research in general toxicology, reproductive toxicology, carcinogenicity, pharmacokinetics and safety pharmacology. The company also carries out research into genetic toxicology, in vitro testing and toxicogenomics.
Its 20,000 sq m (215,000 sq ft) facilities located in Normandy, one hour from Paris, France, house all principal laboratory animal species to the highest standards. Laboratory facilities include analytical chemistry and bioanalysis, clinical pathology, genomics and histology. Support facilities include archives and plant buildings. The company is GLP and AAALAC certified.
More than half the company’s business comes from international customers. Overall, 80 per cent of revenues are in the pharmaceutical and biotechnology sector. Biotechnology and start-up companies alone account for 50 per cent. The company has a world-class team of top-level management in scientific, financial and business activities.
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