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Market Research Report

Monoclonal Antibodies Report Part II: Companies - Holding mAbs in portfolio promises protection against the looming 2011-12 patent cliff

Published by Datamonitor Contact us : +1-860-674-8796
Published 2007/09 Content info 277 pages
Product code DC56815
Price From  US $ 7600 Order/Price list
US $ 7600 PDF by E-mail (Single User License)
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Description TOC

Table of Contents

  • CHAPTER 1 EXECUTIVE SUMMARY
    • Scope of the report
    • Key findings
  • CHAPTER 2 BRIEF OVERVIEW OF UK PRICING & REIMBURSEMENT ENVIRONMENT
    • Introduction
    • The UK uses a range of P&R tools to regulate drug costs and usage
      • Potential future changes to the UK P&R system
      • Additional cost containment tools are used in conjunction with P&R tools
      • The PPRS is the primary mechanism used to control drug prices in the UK
        • Introduction to the PPRS
        • Has the PPRS worked?
        • The future of the PPRS system: is it going to be replaced with value-based pricing?
    • A number of bodies and policies impact drug prescription and spending in the UK
  • CHAPTER 3 NICE: ITS ROLE, EFFECTIVENESS AND ISSUES
    • NICE plays a key role in UK drug reimbursement
      • Introduction: what does NICE do?
      • NICE and pharmacoeconomics
      • How does NICE determine which drugs to assess?
    • A number of issues have been raised with NICE' s appraisal process prompting several reviews
    • Time delays caused by NICE are a significant issue
      • But are time delays a significant issue for drug developers?
      • The solution: there are two key ways to accelerate drug access through improving NICE
        • Earlier guidance can be provided by starting standard appraisals earlier
        • Using STAs should also help to accelerate drug approvals in the future, although they have had limited success so far
    • NICE assessments have created significant controversy
      • NICE has faced significant controversy over its assessment of oncology and Alzheimer' s disease drugs
        • NICE' s controversial decisions over oncology drugs
        • NICE' s guidance over Alzheimer' s disease drugs has also been highly contentious
    • NICE needs to become more responsive
      • NICE has historically faced significant criticism that it is not responsive enough
      • NICE is becoming increasingly responsive to stakeholder activism and consultations
        • NICE changes its mind following consultation
        • Patient, physician and charity activism can help to change NICE responses
    • NICE needs to use assessment factors other than QALYs to make decisions
      • NICE has an over-reliance on QALYs to the detriment of other assessment factors
      • NICE becomes more flexible by offering risk-sharing agreements: the Velcade story
    • Future changes in the influence of NICE
      • Going forward, there is set to be a greater interaction between NICE and other HTA bodies
      • Potential future changes to NICE function and influence
        • Is there a possible role for NICE in drug pricing?
        • NICE guidance set to continue to guide drug provision decisions, yet the government shows greater flexibility in providing access to cheaper drugs
  • CHAPTER 4 BIBLIOGRAPHY
    • Publications and online articles
    • Datamonitor resources
  • APPENDICES
    • Appendix A: Glossary of terms
    • List of Figures
      • Figure 1: A range of P&R tools are in use across 5EU markets, with many of these being used in the UK
      • Figure 2: Regional differences in NICE influence
      • Figure 3: NICE published technology appraisal guidance for drugs has focused heavily on oncology drugs to date
      • Figure 4: NICE topic selection process
      • Figure 5: Datamonitor has identified four key issues that NICE will need to address going forward
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