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020 _z0309116686
035 _a(MiAaPQ)EBC3378368
035 _a(Au-PeEL)EBL3378368
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035 _a(CaONFJC)MIL172680
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040 _aMiAaPQ
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043 _an-us---
050 4 _aRC270.8
_b.I47 2008
082 0 4 _a362.196/994007
_222
245 0 0 _aImproving the quality of cancer clinical trials
_h[electronic resource] :
_bworkshop summary /
_cNational Cancer Policy Forum, Margie Patlack and Sharyl Nass, rapporteurs.
260 _aWashington, D.C. :
_bNational Academies Press,
_cc2008.
300 _axii, 124 p. :
_bill. (some col.).
504 _aIncludes bibliographical references.
505 0 _aIntroduction -- 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.
530 _aAlso available on the World Wide Web.
533 _aElectronic reproduction. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries.
650 0 _aCancer
_xTreatment
_zUnited States.
650 0 _aClinical trials.
655 4 _aElectronic books.
700 1 _aPatlak, Margie.
700 1 _aNass, Sharyl J.
710 2 _aNational Cancer Policy Forum (U.S.)
710 2 _aInstitute of Medicine (U.S.)
710 2 _aProQuest (Firm)
856 4 0 _uhttps://ebookcentral.proquest.com/lib/nird-ebooks/detail.action?docID=3378368
_zClick to View
999 _c31076
_d31076