Phase 0 clinical trials in cancer drug development: from FDA guidance to clinical practice.
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Recommendations for nanomedicine human subjects research oversight: an evolutionary approach for an emerging fieldUnveiling changes in the landscape of patient populations in cancer early drug developmentA phase I trial of veliparib (ABT-888) and temozolomide in children with recurrent CNS tumors: a pediatric brain tumor consortium reportThe role of preclinical animal models in breast cancer drug development.Phase 0 clinical trials: recommendations from the Task Force on Methodology for the Development of Innovative Cancer TherapiesPhase 0 clinical trials in oncology new drug development.Phase 0 Workshop at the 20th EORTC-NCI-AACR Symposium, Geneva.Adoptive T-cell therapy for cancer in the United kingdom: a review of activity for the British Society of Gene and Cell Therapy annual meeting 2015.How can grafted breast cancer models be optimized?Proof of concept to clinical confirmation: evolving clinical trial designs for targeted agents.Designing phase 0 cancer clinical trials.Liquid Chromatographic Determination of NSC 737664 (ABT-888: an Inhibitor of Poly(ADP-ribose) Polymerase (PARP)) in Plasma and Urine in a Phase 0 Clinical TrialEvaluation of surrogate tissues as indicators of drug activity in a melanoma skin modelPhase 0 clinical trial of the poly (ADP-ribose) polymerase inhibitor ABT-888 in patients with advanced malignancies.Phase 0 clinical studies in oncology.The statistics of phase 0 trials.Approaches to phase 1 clinical trial design focused on safety, efficiency, and selected patient populations: a report from the clinical trial design task force of the national cancer institute investigational drug steering committee.Microdosing and Other Phase 0 Clinical Trials: Facilitating Translation in Drug Development.Dose-toxicity models in oncology.Re-overcoming barriers in translating biomarkers to clinical practice.Radiolabeling strategies for tumor-targeting proteinaceous drugs.Therapies for triple negative breast cancer.The application of human phase 0 microdosing trials: A systematic review and perspectives.Circulating tumor DNA for triple-negative breast cancer diagnosis and treatment decisions.Analysis of FDA-approved imaging agents.Role of Phase 0 trials in drug development.Ethical responsibility of phase 0 trials.
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P2860
Phase 0 clinical trials in cancer drug development: from FDA guidance to clinical practice.
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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 December 2007
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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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name
Phase 0 clinical trials in can ...... guidance to clinical practice.
@en
Phase 0 clinical trials in can ...... guidance to clinical practice.
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type
label
Phase 0 clinical trials in can ...... guidance to clinical practice.
@en
Phase 0 clinical trials in can ...... guidance to clinical practice.
@nl
prefLabel
Phase 0 clinical trials in can ...... guidance to clinical practice.
@en
Phase 0 clinical trials in can ...... guidance to clinical practice.
@nl
P2093
P356
P1476
Phase 0 clinical trials in can ...... guidance to clinical practice.
@en
P2093
Alice Chen
Anthony J Murgo
James H Doroshow
Jerry Collins
Joseph E Tomaszewski
Larry Rubinstein
Lee Helman
Martin Gutierrez
Mel Simpson
P304
P356
10.1124/MI.7.6.9
P577
2007-12-01T00:00:00Z