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Incorporating Pharmacogenomics in Clinical Studies

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September 25 - September 26 2006 | Hyatt Regency Baltimore | Baltimore, MD

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Agenda Day Two

Agenda Day Two

DAY TWO: Tuesday September 26, 2006
8:15Morning Coffee
8:45

Chairperson Recap Day One

David Johnston, PhD, Vice President, Chief Scientific Officer, LABCORP

9:00

Clinical Experience
Case Study

A Pharmacogenetic approach to using the Beta Blocker, bucindolol, in Heart Failure

J. David Port, PhD, Vice President Research and Technology, ARCA DISCOVERY

9:45

Practical and Technical Strategies to Incorporate Pharmacogenomics into Clinical Trial Design for Accurate Dosing and Improved Efficacy

Steven Anderson, PhD, Director and Chief Scientific Officer,
VIROMED

10:30Morning Break and Hotel Checkout
11:00

Outsourcing Clinical Trials Pharmacogenomic Sample Preparation, Management and Testing

Andrea Pay, PhD, Senior Clinical Scientist, Scientific Affairs,
QUEST DIAGNOSTICS

12:00

Networking Luncheon

1:15

Voluntary Genomic Data Submission-Case Study
Pharmacogenomic Testing: Opportunities and Challenges to Implementation

Steve McPhail, PhD, President and Chief Executive Officer,
EXPRESSION ANALYSIS

2:00

Understanding and Overcoming Challenges in Diagnostic Co-Development

Please contact Anne Reel at areel@iirusa.com

2:45

Panel Discussion
Overcoming Challenges for Successful Trials Using Pharmacogenomics

Andrea Pay, PhD, Senior Clinical Scientist, Scientific Affairs,
QUEST DIAGNOSTICS

Steve McPhail, PhD President and Chief Executive Officer
EXPRESSION ANALYSIS

Luis Parodi, PhD, Director and Site Head, Clinical Pharmacogenomics,
PFIZER

3:30

Conference Concludes



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