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dc.contributor.authorBenson, Cen_US
dc.contributor.authorWhite, Jen_US
dc.contributor.authorDe Bono, JSen_US
dc.contributor.authorO'Donnell, Aen_US
dc.contributor.authorRaynaud, Fen_US
dc.contributor.authorCruickshank, Cen_US
dc.contributor.authorMcGrath, Hen_US
dc.contributor.authorFrenz, Len_US
dc.contributor.authorRose, Fen_US
dc.contributor.authorWalton, Men_US
dc.contributor.authorWorkman, Pen_US
dc.contributor.authorKaye, Sen_US
dc.date.accessioned2017-03-24T14:20:48Z
dc.identifier.citationBr J Cancer. 2007, Jan 15, 1 (96), pp. 29 - 37en_US
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/496
dc.format.extent29 - 37en_US
dc.titleA phase I trial of the selective oral cyclin-dependent kinase inhibitor seliciclib (CYC202;R-Roscovitine), administered twice daily for 7-days every 21 days.en_US
dc.typeJournal Article
dcterms.dateAccepted2006-11-07en_US
rioxxterms.licenseref.startdate2006-11-07en_US
rioxxterms.typeJournal Article/Reviewen_US
dc.relation.isPartOfBr J Cancer. 2007en_US
pubs.editionJan 15en_US
pubs.issue96en_US
pubs.notesNo embargoen_US
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Clinical Pharmacology & Trials (including Drug Metabolism & Pharmacokinetics Group)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Closed research teams/Medicine Drug Development Unit (Kaye)
pubs.publication-statusAccepteden_US
pubs.volume1en_US
pubs.embargo.termsNo embargoen_US
icr.researchteamClinical Pharmacology & Trials (including Drug Metabolism & Pharmacokinetics Group)en_US
icr.researchteamMedicine Drug Development Unit (Kaye)en_US
dc.contributor.icrauthorRaynaud, Florenceen_US
dc.contributor.icrauthorWorkman, Paulen_US
dc.contributor.icrauthorKaye, Stanley Bernarden_US


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