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dc.contributor.authorLassen, U
dc.contributor.authorChinot, O
dc.contributor.authorMcBain, Catherine A
dc.contributor.authorMau-Sørensen, M
dc.contributor.authorLarsen, V
dc.contributor.authorBarrie, M
dc.contributor.authorRoth, P
dc.contributor.authorKrieter, O
dc.contributor.authorWang, K
dc.contributor.authorHabben, K
dc.contributor.authorTessier, J
dc.contributor.authorLahr, A
dc.contributor.authorWeller, M
dc.date.accessioned2015-02-25T11:57:20Z
dc.date.available2015-02-25T11:57:20Z
dc.date.issued2015-02-09
dc.identifier.citationPhase 1 dose-escalation study of the antiplacental growth factor monoclonal antibody RO5323441 combined with bevacizumab in patients with recurrent glioblastoma. 2015: Neuro-oncologyen
dc.identifier.issn1523-5866
dc.identifier.pmid25665807
dc.identifier.doi10.1093/neuonc/nov019
dc.identifier.urihttp://hdl.handle.net/10541/345296
dc.description.abstractWe conducted a phase 1 dose-escalation study of RO5323441, a novel antiplacental growth factor (PlGF) monoclonal antibody, to establish the recommended dose for use with bevacizumab and to investigate the pharmacokinetics, pharmacodynamics, safety/tolerability, and preliminary clinical efficacy of the combination.
dc.languageENG
dc.language.isoenen
dc.rightsArchived with thanks to Neuro-oncologyen
dc.titlePhase 1 dose-escalation study of the antiplacental growth factor monoclonal antibody RO5323441 combined with bevacizumab in patients with recurrent glioblastoma.en
dc.typeArticleen
dc.contributor.departmentDepartment of Oncology, Rigshospitalet, Copenhagen, Denmarken
dc.identifier.journalNeuro-oncologyen
html.description.abstractWe conducted a phase 1 dose-escalation study of RO5323441, a novel antiplacental growth factor (PlGF) monoclonal antibody, to establish the recommended dose for use with bevacizumab and to investigate the pharmacokinetics, pharmacodynamics, safety/tolerability, and preliminary clinical efficacy of the combination.


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