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Market Research Report

Powering Discovery through Target Evaluation: Moving Beyond the Validation Paradigm

Published by Insight Pharma Reports Contact us : +1-860-674-8796
Published 2005/08 Content info 114 pages
Product code CD32095
Price From  US $ 2750 Order/Price list
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Description TOC

Abstract

The shift from traditional to genomics-and proteomics-based drug discovery has fundamentally changed the way researchers view the subject of targets. After decades of focusing on a few hundred relatively well-characterized therapeutic targets, drug developers are now finding that the genomics revolution has presented them with the opposite dilemma: thousands of prospective targets about which little is known. Powering Discovery through Target Evaluation: Moving beyond the Validation Paradigm comprehensively evaluates current efforts to solve the target validation problem.

With steadily growing drug development costs, depleted pipelines, and few blockbusters on the horizon, the ability to quickly identify the most biologically promising of these targets will be the single-largest differentiator between the winners and losers within the research-based pharmaceutical industry over the next decade. Target validation thus becomes the central issue in the success or failure of pharmaceutical R&D. Researchers must find the means to choose the best drug targets early in the process to reduce costly attrition rates and allow for more efficient drug discovery and development.

Powering Discovery through Target Evaluation: Moving beyond the Validation Paradigm offers unique and insightful analysis of current efforts to sift through the post-genomic data deluge, prioritize targets, and optimize resources to develop the most promising leads. This report:

  • Reviews the key issues with the current target validation paradigm.
  • Evaluates the tools and business strategies of select companies competing in this arena.
  • Analyzes efforts to use proteomic techniques for target validation.
  • Addresses applications of RNAi technology to target validation and pathway mapping.
  • Examines the issue of multiple molecular "causes" of disease by developing therapies (including single drugs and combination therapies) that address more than one molecular target.
  • Discusses whole pathway approaches to drug discovery--a crucial step toward understanding the function of poorly characterized targets. Pathway analysis may also be important in patient stratification.
  • Evaluates the current status of translational medicine as a strategy for improving the productivity of drug development.
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