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American Association of Pharmaceutical Scientists National Biotechnology Conference Short Course: Translational Challenges in Developing Antibody-Drug Conjugates: May 24, 2012, San Diego,CA
Authors:Karen Thudium  Sanela Bilic  Douglas Leipold  William Mallet  Surinder Kaur  Bernd Meibohm  Hans Erickson  Jay Tibbitts  Hong Zhao  Manish Gupta
Institution:1.Novartis Pharmaceuticals; Clinical Pharmacology; Oncology Business Unit; Florham Park, NJ USA;2.Genentech; South San Francisco, CA USA;3.Novartis Institutes for BioMedical Research; Emeryville, CA USA;4.The University of Tennessee Heath Science Center; College of Pharmacy; Memphis, TN USA;5.ImmunoGen, Inc.; Waltham, MA USA;6.U.S. Food and Drug Administration; Silver Spring, MD USA;7.Bristol-Myers Squibb Company; New Brunswick, NJ USA
Abstract:The American Association of Pharmaceutical Scientists (AAPS) National Biotechnology Conference Short Course “Translational Challenges in Developing Antibody-Drug Conjugates (ADCs),” held May 24, 2012 in San Diego, CA, was organized by members of the Pharmacokinetics, Pharmacodynamics and Drug Metabolism section of AAPS. Representatives from the pharmaceutical industry, regulatory authorities, and academia in the US and Europe attended this short course to discuss the translational challenges in ADC development and the importance of characterizing these molecules early in development to achieve therapeutic utility in patients. Other areas of discussion included selection of target antigens; characterization of absorption, distribution, metabolism, and excretion; assay development and hot topics like regulatory perspectives and the role of pharmacometrics in ADC development. MUC16-targeted ADCs were discussed to illustrate challenges in preclinical development; experiences with trastuzumab emtansine (T-DM1; Genentech) and the recently approved brentuximab vedotin (Adcetris®; Seattle Genetics) were presented in depth to demonstrate considerations in clinical development. The views expressed in this report are those of the participants and do not necessarily represent those of their affiliations.
Keywords:ADC  pharmacokinetics  linker  trastuzumab emtansine  brentuximab vedotin
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