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The Role of Modern Biology and Medicine in Drug Development in
Academia and Industry
Sponsored by the Society for Experimental
Biology and Medicine
Sun. April 2—3:15-5:15 PM
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| Chaired: |
Charles A. Blake,
Univ. of South Carolina Sch. of Med.
Kenneth L. Barker, State Univ. of New York, Syracruse |
Drug development is a complex process that routinely
involves effective collaborations between academic and physician scientists
and industry. This symposium addresses careers in the drug development
industry, the performance of translational research in academia and
industry, and a multitude of factors involved in collaborations essential to
the drug discovery and development process. First, Ted Love will discuss
competing occupational advantages affecting recruitment of scientists and
physicians needed in drug development programs in industry; ideal
backgrounds for successful applicants for positions in industry in drug
development; ethical and regulatory considerations affecting the performance
of scientists and physicians in drug development programs in industry and in
other organizations such as the National Institutes of Health and
universities; and the nature of gratifications available to scientists in
industry working on drug development. Timothy Clackson will focus on
similarities and differences entailed in the performance of translational
research in academia and in industry. Logistic, operational, and scientific
oversights are complex, especially because they often involve relationships
with clinical enterprises outside of the corporate structure itself and the
use of laboratory animals. The nature of effective relationships in
multiple settings will be addressed with examples of development of specific
types of therapeutic agents. Scott Kennedy will then describe the long road
from formulation of a good discovery idea to acceptance of a new drug in the
marketplace. He will focus on the importance of collaborations and
partnerships in this process. These partnerships help increase confidence
and improve decision making on issues of safety and efficacy pre-clinically,
that can reduce attrition and expedite providing new quality drugs to
patients faster and at lower costs. Collaborations involve addressing
multiple issues that include infrastructure, safety, regulatory matters,
intellectual property, technical and personnel considerations, source
document capture and data analysis issues, and legal and strategic
alliances. This symposium will be of special interest to scientists and
physicians in all fields who have interest in working for or collaborating
with the pharmaceutical drug industry.
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3:15 PM |
How to attract the best and the brightest
to benefit drug development programs.
Ted W. Love, Nuvelo, Inc.
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3:45 PM |
Translational research in academia and
industry.
Timothy P. Clackson, ARIAD Pharmaceuticals, Inc.
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4:15 PM |
Effective Partnering of Academic and
Physician Scientists with the Pharmaceutical Drug Development Industry
Scott P. Kennedy, Pfizer Global Research & Development
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4:45 PM |
General discussion.
Burton E. Sobel, Univ. of Vermont
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