rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
5
|
pubmed:dateCreated |
2003-4-18
|
pubmed:abstractText |
The aim of this study was to assess the feasibility of administering bizelesin, a cyclopropylpyrroloindole with extraordinarily high potency as a bifunctional DNA-damaging agent and selectivity for specific AT-rich DNA sequences, as a single i.v. bolus injection every 4 weeks in patients with advanced solid malignancies. The study also sought to determine the maximum tolerated dose (MTD) of bizelesin, characterize its pharmacokinetic behavior, and seek preliminary evidence of anticancer activity.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
May
|
pubmed:issn |
0923-7534
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
14
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
775-82
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:12702533-Adult,
pubmed-meshheading:12702533-Aged,
pubmed-meshheading:12702533-Aged, 80 and over,
pubmed-meshheading:12702533-Antineoplastic Agents, Alkylating,
pubmed-meshheading:12702533-DNA,
pubmed-meshheading:12702533-Dose-Response Relationship, Drug,
pubmed-meshheading:12702533-Drug Administration Schedule,
pubmed-meshheading:12702533-Female,
pubmed-meshheading:12702533-Humans,
pubmed-meshheading:12702533-Indoles,
pubmed-meshheading:12702533-Intercalating Agents,
pubmed-meshheading:12702533-Male,
pubmed-meshheading:12702533-Middle Aged,
pubmed-meshheading:12702533-Neoplasms,
pubmed-meshheading:12702533-Urea
|
pubmed:year |
2003
|
pubmed:articleTitle |
A phase I study of bizelesin, a highly potent and selective DNA-interactive agent, in patients with advanced solid malignancies.
|
pubmed:affiliation |
Brooke Army Medical Center, San Antonio, TX 78229, USA.
|
pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, U.S. Gov't, P.H.S.,
Clinical Trial, Phase I
|