Für diesen Artikel ist leider kein Bild verfügbar.

Anticancer Drug Development Guide

Preclinical Screening, Clinical Trials, and Approval

Beverly A. Teicher (Herausgeber)

Buch | Hardcover
336 Seiten
1997 | Revised ed.
Humana Press Inc. (Verlag)
978-0-89603-461-7 (ISBN)
85,55 inkl. MwSt
  • Titel ist leider vergriffen;
    keine Neuauflage
  • Artikel merken
This work analyzes the processes for the numerous steps involved in preclinical and clincial screening and approval of anticancer agents. It should be of interest to pharmacologists and oncologists.
Experienced cancer researchers from pharmaceutical companies, government laboratories, and academia comprehensively review and describe the arduous process of cancer drug discovery and approval. They focus on using preclinical in vivo and in vitro methods to identify molecules of interest, detailing the targets and criteria for success in each type of testing and defining the value of the information obtained from the various tests. They also define each stage of clinical testing, explain the criteria for success, and outline the requirements for FDA approval. A companion volume by the same editor (Cancer Therapeutics: Experimental and Clinical Agents) reviews existing anticancer drugs and potential anticancer therapies. These two volumes in the Cancer Drug Discovery and Development series reveal how and why molecules become anticancer drugs and thus offer a blueprint for the present and the future of the field.

Part I. In Vitro Methods. High-Volume Screening, Michel Page. The NCI In Vitro Anticancer Drug Discovery Screen: Concept, Implementation, and Operation, 1985-1995, Michael R. Boyd. Human Tumor Screening, Axel-R. Hanauske, Susan G. Hilsenbeck, and Daniel D. Von Hoff. Part II. In Vivo Methods. Murine L1210 and P388 Leukemias, William R. Waud. In Vivo Methods for Screening and Preclinical Testing: Use of Rodent Solid Tumors for Drug Discovery, Thomas Corbett, Fred Valeriote, Patricia LoRusso, Lisa Polin, Chiab Panchapor, Susan Pugh, Kathryn White, Juiwanna Knight, Lisa Demchik, Julie Jones, Lynne Jones, and Loretta Lisow. Human Tumor Xenograft Models in NCI Drug Development, Jaqueline Plowman, Donald J. Dykes, Melinda Hollingshead, Linda Simpson-Herren, and Michael C. Alley. Fertile Seed and Rich Soil: The Development of Clinically Relevant Models of Human Cancer by Surgical Orthotopic Implantation of Intact Tissue, Robert M. Hoffman. Preclinical Models for High-Dose Therapy, Beverly A. Teicher. Models for Minimal Residual Tumor, Beverly A. Teicher. Spontaneously Occurring Tumors in Companion Animals as Models for Drug Development, David M. Vail and E. Gregory MacEwen. Part III. Clinical Testing. Working with the National Cancer Institute, Edward A. Sausville. Phase I Trial Design and Methodology, Deborah L. Toppmeyer. Phase II Clinical Trials in Oncology, Christine Khater, Paul Laub, James M. Gallo, Andre Rogatko, and Peter J. O'Dwyer. Drug Development in Europe, Thomas Anthony Connors and Herbert M. Pinedo. The Phase III Cancer Clinical Trial, Emil Frei III. FDA Role in Cancer Drug Development and Requirements for Approval, Robert L. Justice. Index

Reihe/Serie Cancer Drug Discovery and Development
Verlagsort Totowa, NJ
Sprache englisch
Maße 254 x 178 mm
Gewicht 1128 g
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete Onkologie
Medizin / Pharmazie Medizinische Fachgebiete Pharmakologie / Pharmakotherapie
ISBN-10 0-89603-461-5 / 0896034615
ISBN-13 978-0-89603-461-7 / 9780896034617
Zustand Neuware
Haben Sie eine Frage zum Produkt?
Mehr entdecken
aus dem Bereich

von Hannes Leischner

Buch | Softcover (2023)
Urban & Fischer in Elsevier (Verlag)
27,00
Resilienz innovativ stärken : ein Praxishandbuch

von Christa Diegelmann; Margarete Isermann; Tanja Zimmermann

Buch | Softcover (2023)
Kohlhammer (Verlag)
36,00