Reducing Late Stage Drug Attrition By Employing Predictive Toxicology To Maximise Drug Candidate Success

Pharma IQ is delighted to announce the dates for the 2nd Annual Predictive Toxicology Conference taking place in London on the 24th-25th February 2010. Predictive Toxicology is a constantly evolving area of R&D, helping to reduce costs and increase efficiency of drug development through ever more innovative technologies to ultimately ensure that pipeline compounds pass legislation and become safe, profit-making drugs.

Industry and Regulatory professional will share their expertise to help you:

  • Increase the predictability of your approaches through improved interpretation and implementation of existing and new Predictive Toxicology technologies in order to increase the percentage of drug candidates that are successful. Insights from the FDA and Pfizer.
  • Benchmark your companies’ existing strategies with case studies highlighting the benefits of the technology within the various divisions of prediction from GSK, Abbott and UCB-pharma.
  • Ensure compliance by understanding the positioning of the new technologies and assays within legislation set by regulatory bodies to achieve first time approval, with the MHRA and European Commission.
  • Stay ahead of the competition by learning about the future of Predictive Toxicology- genetic toxicology and stem cells? with the FDA and Astrazeneca

TOP RATED SPEAKERS INCLUDE:

  • Dr Eric Blomme
    Director of Investigative Toxicology
    Abbott
  • Dr Martha Moore
    Director, Division of Genetic and Reproductive Toxicology
    FDA
  • Dr James Dykens
    Associate Research Fellow, Drug Safety R&D
    Pfizer
  • Dr Andrew Worth
    Project Leader Computational Toxicology, Systems Toxicology Unit Institute for Health and Consumer Protection (IHCP)
    European Commission - Joint Research Centre
  • Constantine Kreatsoulas
    Senior Research Chemist
    Chemical Modelling and Informatics Group Merck & Co.
  • Dr David Jones
    Principle Scientific Officer
    MHRA

What Your Peers Think...

"In today's pharmaceutical environment two themes predominate, patient safety and probability of technical success. As development of new pharmaceuticals becomes more and more time consuming and expensive, any and all approaches which can identify potential problems must be explored. At the Predictive Toxicology Conference 2010, the aim is to provide attendees with practical knowledge which translates to better patient outcomes and better returns on investment"
Dr Mitchell Friedman- Director of Toxicology, Takeda Pharmaceuticals
'Late stage attrition of nascent drugs causes substantial losses, both financially and in terms of effort. Conversely, establishing assays with high false positive rates needlessly eliminates compounds that might well have been efficacious and safe in humans. De-risking strategies that predict clinical disposition are the ideal towards which we are moving; we need compounds to fail early, but for the right reasons. Recent advances on several fronts are providing in silico, cellular and animal models that more faithfully predict clinical reality. I am speaking at Predictive Toxicology again this year to help keep attention focused on mitochondrial dysfunction as a key safety issue, but also to hear about the latest developments on other fronts."
Dr James Dykens- Associate Research Fellow, Drug Safety R&D, Pfizer
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