Table of Contents
- Strategic Considerations
- Stakeholder Implications
- Overview of Pharmaceutical R&D
- Tactical Uses of High-Throughput and High-Content Technologies
- Decreasing Cycle Times and Costs
- Lead Identifi cation Technologies
- Target Identifi cation and Validation Technologies
- Strategic Uses of High-Throughput and High-Content Technologies
- Learning from Approved Drugs
- Integrating RNA Signature Profi les with Drugs, Cellular Mechanisms,
and Disease
- Predicting Target Druggability
- Chemical Filters
- Predictive Toxicology
- Patient-Specifi c Therapies
- New Ways to Perform Clinical Trials
- Organizational and Operational Strategies
- Team Approaches to Drug Discovery and Development
- GlaxoSmithKline
- Merck
- Roche
- Novartis
- Wyeth
- Information Sharing
- External Sources of Innovation
- Academic Resources
- Biotechnology Companies
- Pharmaceutical Venture Capital
- Outlook for Pharmaceutical R&D
Tables
- 1. FDA-Approved Drugs Derived from Combinatorial Chemistry and/or
High-Throughput Screening
- 2. Select Clinical Candidates Derived from Target Identifi cation or
Validation Programs
- 3. Select Biomarkers Included in FDA-Approved Drug Labels
- 4. Comparison of Conventional and Adaptive Clinical Trials
- 5. Select Pharmaceutical Research and R&D Centers
- 6. Select Pharmaceutical Drugs Originating from Biotechnology Companies
- 7. Select Pharmaceutical/Biotechnology Venture Capital Funds
Figures
- 1. FDA New Molecular Entity Approvals, 1990-2007, vs. R&D Spending by
PhRMA Members, 1990-2006
- 2. Drug Development Models: Conventional Development vs. Translation and
Experimental Medicine
- 3. Comparison of Pharmaceutical R&D Structures During Discovery and
Development
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