Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2004-2-4
pubmed:abstractText
PKC412 (N-benzoyl-staurosporine), an oral inhibitor of protein kinase C, is capable of cell cycle inhibition and is endowed with anti-angiogenic properties. This dose-finding phase I study was designed to establish the maximum tolerated dose (MTD) of PKC412 when combined with cisplatin-gemcitabine.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0923-7534
pubmed:author
pubmed:issnType
Print
pubmed:volume
15
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
316-23
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:14760128-Administration, Oral, pubmed-meshheading:14760128-Adult, pubmed-meshheading:14760128-Aged, pubmed-meshheading:14760128-Angiogenesis Inhibitors, pubmed-meshheading:14760128-Antineoplastic Combined Chemotherapy Protocols, pubmed-meshheading:14760128-Asthenia, pubmed-meshheading:14760128-Carcinoma, Non-Small-Cell Lung, pubmed-meshheading:14760128-Cisplatin, pubmed-meshheading:14760128-Deoxycytidine, pubmed-meshheading:14760128-Diarrhea, pubmed-meshheading:14760128-Enzyme Inhibitors, pubmed-meshheading:14760128-Female, pubmed-meshheading:14760128-Humans, pubmed-meshheading:14760128-Infusions, Intravenous, pubmed-meshheading:14760128-Lung Neoplasms, pubmed-meshheading:14760128-Male, pubmed-meshheading:14760128-Maximum Tolerated Dose, pubmed-meshheading:14760128-Middle Aged, pubmed-meshheading:14760128-Protein Kinase C, pubmed-meshheading:14760128-Staurosporine
pubmed:year
2004
pubmed:articleTitle
Phase I study of PKC412 (N-benzoyl-staurosporine), a novel oral protein kinase C inhibitor, combined with gemcitabine and cisplatin in patients with non-small-cell lung cancer.
pubmed:affiliation
Department of Medicine, Institut Gustave-Roussy, Villejuif, France.
pubmed:publicationType
Journal Article, Clinical Trial, Research Support, Non-U.S. Gov't, Clinical Trial, Phase I