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pubmed-article:20805300pubmed:dateCreated2010-10-4lld:pubmed
pubmed-article:20805300pubmed:abstractTextAntibody drug conjugates (ADCs) combine the ideal properties of both antibodies and cytotoxic drugs by targeting potent drugs to the antigen-expressing tumor cells, thereby enhancing their antitumor activity. Successful ADC development for a given target antigen depends on optimization of antibody selection, linker stability, cytotoxic drug potency, and mode of linker-drug conjugation to the antibody. Here, we systematically examined the in vitro potency as well as in vivo preclinical efficacy and safety profiles of a heterogeneous preparation of conventional trastuzumab-mcc-DM1 (TMAb-mcc-DM1) ADC with that of a homogeneous engineered thio-trastuzumab-mpeo-DM1 (thioTMAb-mpeo-DM1) conjugate. Experimental Design andlld:pubmed
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pubmed-article:20805300pubmed:articleTitleEngineered thio-trastuzumab-DM1 conjugate with an improved therapeutic index to target human epidermal growth factor receptor 2-positive breast cancer.lld:pubmed
pubmed-article:20805300pubmed:affiliationGenentech, Inc., South San Francisco, California 94080, USA. jagath@gene.comlld:pubmed
pubmed-article:20805300pubmed:publicationTypeJournal Articlelld:pubmed