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Titlebook: Anticancer Drug Development Guide; Preclinical Screenin Beverly A. Teicher Book 1997 Springer Science+Business Media New York 1997 cancer.c

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Betriebs- und Wirtschaftsinformatikcal trial groups, or as part of the activities of Phase I and II cooperative agreement organizations. CTEP also monitors the conduct of these studies as well as Phase III studies focusing on the optimal use of currently available FDA-approved agents.
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High-Volume Screeningan important role in drug evaluation, but with the development of a large number of cytotoxic drugs, animal models are too costly and the delay is too long for these models to be used for large-scale screening.
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Human Tumor Xenograft Models in NCI Drug Developmenthave been summarized recently (.). Test procedures are designed to provide comparative quantitative data, which in turn, permit selection of the best candidate agents from a given chemical or biological class. Periodic, comprehensive reviews by various NCI committees serve not only to identify and e
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Fertile Seed and Rich Soilf cancer to test and investigate the hypothesis of Paget, as well as for treatment discovery. Thus, there has been a critical need in cancer treatment and research for rodent models that are clinically relevant. Ideal models would allow the transplantation of the majority of human tumors, such that
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