Reminder: Dr. Maurer's webinar next week
This is a reminder that Dr. Maurer's webinar Translational Modeling &
Simulation in Support of Rational Drug Discovery: Principles, Challenges, and
Examples will take place on December 13, 2011 at 1:00 pm EST (GMT -5:00).
One of the most serious threats to sustained pharmaceutical innovation is the
rapidly rising cost of research and development experienced over the past
several decades. This exponential rise in cost has been attributed to a variety
of factors including increasing technology investments, rising regulatory and
commercial hurdles, and higher attrition rates. Among these factors, attrition
due to insufficient efficacy and / or safety stands out as a major contributor.
Historically high rates of efficacy and safety related attrition suggest that
that there is often insufficient knowledge upon which critical decisions in
drug discovery are made, namely: which biochemical targets to pursue and which
chemical matter to bring forward into the clinic. Preclinical modeling and
simulation (e.g. systems biology, PK/PD) is a useful approach to integrating
biological information toward the selection of the most promising targets and
the design of the most promising chemical matter. As such, over the past
several years, quantitative modeling and simulation has become increasingly
popular among pharmaceutical companies seeking to reduce attrition. This
presentation will provide the rationale for quantitative modeling and
simulation, guiding principles for successful implementation of fit for purpose
models, and examples illustrative of value added in drug discovery.
Dr. Maurer's presentation is a part of the monthly world-wide webinar series
“Impact of Modeling & Simulation in Drug Development” hosted by Rosa & Co. LLC.
The purpose of the “Impact” series is to foster the use of M&S activities in
all phases of drug development by illustrating the advantages and enhancing the
applicability of M&S in product discovery, development, and marketing programs.
The series is intended for drug development project team members from discovery
to phase 4 clinical trials. This includes pharmacologists, ADME scientists,
PK/PD modelers, clinical pharmacologists, clinical development team members,
regulatory affairs specialists, and other interested professionals.
Register for this free webinar at www.rosaandco.com/webinar. After registering
you will receive a confirmation email containing information about joining the
webinar. More information about the webinar series, an archive of past
webinars, and a list of future webinar speakers may be found at
www.rosaandco.com/webinar.
Please allow 5-10 minutes for a Java applet to be installed on your computer
prior to joining our webinar series for the first time.
Toufigh Gordi, PhD
President, PK/PD and Clinical Pharmacology Services
Rosa & Co. LLC: www.rosaandco.com
E-mail: [email protected]
Tel.: 408-480-7314
Fax: 408-370-9810
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