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dc.contributor.authorIllidge, Timothy M
dc.contributor.authorCheadle, Eleanor J
dc.contributor.authorDonaghy, Clare
dc.contributor.authorHoneychurch, Jamie
dc.date.accessioned2014-10-08T10:08:00Z
dc.date.available2014-10-08T10:08:00Z
dc.date.issued2014-10
dc.identifier.citationUpdate on obinutuzumab in the treatment of B-cell malignancies. 2014, 14 (10):1507-17 Expert Opin Biol Theren
dc.identifier.issn1744-7682
dc.identifier.pmid25190612
dc.identifier.doi10.1517/14712598.2014.948414
dc.identifier.urihttp://hdl.handle.net/10541/332335
dc.description.abstractThe anti-CD20 mAb rituximab has revolutionized the treatment of B-cell malignancies, improving outcome for patients. Despite these improvements, the majority of patients still relapse and become refractory to rituximab. Further efforts to improve anti-CD20 mAb efficacy have recently focused on obinutuzumab /GA101, a novel anti-CD20 mAb glycoengineered to display enhanced Fc-mediated effector mechanisms and induce direct cell death.
dc.language.isoenen
dc.rightsArchived with thanks to Expert opinion on biological therapyen
dc.titleUpdate on obinutuzumab in the treatment of B-cell malignancies.en
dc.typeArticleen
dc.contributor.departmentUniversity of Manchester, Institute of Cancer Sciences, The Christie Hospital, Manchester Cancer Research Centre, Manchester Academic Health Sciences Centre , Manchester M20 4BX , UK +44 0 161 446 8110 ; +44 0 161 446 8001 ; tmi@manchester.ac.uk.en
dc.identifier.journalExpert Opinion on Biological Therapyen
dc.description.collectionLymphoma Research Teamen
html.description.abstractThe anti-CD20 mAb rituximab has revolutionized the treatment of B-cell malignancies, improving outcome for patients. Despite these improvements, the majority of patients still relapse and become refractory to rituximab. Further efforts to improve anti-CD20 mAb efficacy have recently focused on obinutuzumab /GA101, a novel anti-CD20 mAb glycoengineered to display enhanced Fc-mediated effector mechanisms and induce direct cell death.


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