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Improving the quality of cancer clinical trials workshop summary /

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Bibliografiske detaljer
Corporate Authors: National Cancer Policy Forum (U.S.), Institute of Medicine (U.S.), ebrary, Inc
Andre forfattere: Patlak, Margie, Nass, Sharyl J.
Format: Electronisk eBog
Sprog:engelsk
Udgivet: Washington, D.C. : National Academies Press, c2008.
Fag:
Cancer > Treatment > United States.
Clinical trials.
Electronic books.
Online adgang:An electronic book accessible through the World Wide Web; click to view
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Indholdsfortegnelse:
  • Introduction
  • New clinical trial designs. Phase 0 trials
  • Adaptive trial designs
  • Targeting multiple pathways with multiple drugs
  • Preclinical model systems
  • Molecular imaging. Current and developing methods
  • Challenges of molecular imaging
  • Screening for predictive markers. The challenges of clinical validation
  • Bioimaging predictive markers
  • Clinical translation
  • Panel discussion
  • Costs of clinical trials. Regulatory costs
  • Patient accrual
  • Global outsourcing
  • Time is money
  • Public-private collaborations
  • Regulatory issues. Regulatory barriers to innovation
  • Patient advocacy perspective
  • Regulation of in vitro diagnostics
  • Regulatory issues in improving cancer clinical trials
  • Reports from the case study discussion groups. Adaptive trial design
  • Phase 0 trials
  • Imaging
  • Use of proteomics/genomics to assign therapy in lung cancer
  • Use of genetics/genomics to assign therapy.

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