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dc.contributor.authorWheate, Nial J.
dc.contributor.authorWalker, Shonagh
dc.contributor.authorCraig, Gemma E.
dc.contributor.authorOun, Rabbab
dc.date.accessioned2013-07-23
dc.date.available2013-07-23
dc.date.issued2010-06-30
dc.identifier.citationDalton Trans., 2010, 39, 8113-8127en
dc.identifier.urihttp://hdl.handle.net/2123/9269
dc.description.abstractSince its approval in 1979 cisplatin has become an important component in chemotherapy regimes for the treatment of ovarian, testicular, lung and bladder cancers, as well as lymphomas, myelomas and melanoma. Unfortunately its continued use is greatly limited by severe dose limiting side effects and intrinsic or acquired drug resistance. Over the last 30 years, 23 other platinum-based drugs have entered clinical trials with only two (carboplatin and oxaliplatin) of these gaining international marketing approval, and another three (nedaplatin, lobaplatin and heptaplatin) gaining approval in individual nations. During this time there have been more failures than successes with the development of 14 drugs being halted during clinical trials. Currently there are four drugs in the various phases of clinical trial (satraplatin, picoplatin, LipoplatinTM and ProLindacTM). No new small molecule platinum drug has entered clinical trials since 1999 which is representative of a shift in focus away from drug design and towards drug delivery in the last decade. In this perspective article we update the status of platinum anticancer drugs currently approved for use, those undergoing clinical trials and those discontinued during clinical trials, and discuss the results in the context of where we believe the field will develop over the next decade.en
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.rightsOther
dc.subjectcisplatinen
dc.subjectoxaliplatinen
dc.subjectBBR3464en
dc.subjectnedaplatinen
dc.subjectlobaplatinen
dc.subjectcarboplatinen
dc.subjectpicoplatinen
dc.subjectsatraplatinen
dc.titleThe status of platinum anticancer drugs in the clinic and in clinical trialsen
dc.typeArticleen
dc.identifier.doi10.1039/c0dt00292e
dc.type.pubtypePublisher's versionen
usyd.facultyFaculty of Medicine and Health, Sydney Pharmacy Schoolen


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