Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
about
Achieving sufficient accrual to address the primary endpoint in phase III clinical trials from U.S. Cooperative Oncology GroupsData for cancer comparative effectiveness research: past, present, and future potential.Routine data from hospital information systems can support patient recruitment for clinical studies.Common metrics to assess the efficiency of clinical research.Time spent for activation of non-profit studies in oncology in Italy.Evaluating protocol lifecycle time intervals in HIV/AIDS clinical trials.Harmonization of the practice of independent ethics committees in Italy: project E-submission.A sense of urgency: Evaluating the link between clinical trial development time and the accrual performance of cancer therapy evaluation program (NCI-CTEP) sponsored studies.Phase III clinical trial development: a process of chutes and laddersIntegrating utilization-focused evaluation with business process modeling for clinical research improvementBarriers to recruitment of rural patients in cancer clinical trials.Evaluating translational research: a process marker modelSponsors meet scientists to speed pediatric medicines developmentDeveloping Common Metrics for the Clinical and Translational Science Awards (CTSAs): Lessons Learned.Therapeutic hypothermia after pediatric cardiac arrest trials: the vanguard phase experience and implications for other trials.Activating clinical trials: a process improvement approachProtocol Development Program: A Novel Approach to Overcoming Barriers to Clinical Research.Modeling the dissemination and uptake of clinical trials results.Cancer drugs in the United States: Justum Pretium--the just priceImpact of NCI-mandated scientific review on protocol development and content.Gynecologic oncology group strategies to improve timeliness of publication.Quasi-random reflections on randomized controlled trials and comparative effectiveness research.Building a statewide clinical trials network for cancer care in West Virginia.Cancer research in the United States: dying by a thousand paper cuts.Institutional Scientific Review of Cancer Clinical Research Protocols: A Unique Requirement That Affects Activation Timelines.Barriers to Cancer Clinical Trial Participation Among Saudi Nationals: A Cross-Sectional Study.Time required to start multicentre clinical trials within the Italian Medicine Agency programme of support for independent research.Setting up a clinical trial for a novel disease: a case study of the Doxycycline for the Treatment of Nodding Syndrome Trial - challenges, enablers and lessons learned.Meeting the Challenge: The National Cancer Institute's Central Institutional Review Board for Multi-Site Research.
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P2860
Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 02 March 2009
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
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Steps and time to process clinical trials at the Cancer Therapy Evaluation Program.
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Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
@en
Steps and time to process clinical trials at the Cancer Therapy Evaluation Program.
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Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
@en
Steps and time to process clinical trials at the Cancer Therapy Evaluation Program.
@nl
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P2860
P356
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Steps and time to process clinical trials at the Cancer Therapy Evaluation Program
@en
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Alan B Sandler
David M Dilts
Jeffrey Abrams
Joshua S Crites
Lori B Ferranti
Margaret Mooney
Shanda Finnigan
Steven Friedman
Steven K Cheng
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P304
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10.1200/JCO.2008.19.9133
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P577
2009-03-02T00:00:00Z