Phase 1 trial and assay of rubidazone (NSC 164011) in patients with advanced solid tumors.

Abstract:

:A new high-pressure liquid chromatographic method was developed for the simultaneous determination of rubidazone and daunorubicin in human plasma at concentrations as low as 60 ng/ml. Clinical toxicity and the stability of rubidazone were studied in nine patients with advanced solid tumors. Rubidazone was administered by i.v. infusion over 1 hr on a single day every 4 weeks. Moderate leukopenia was the dose-limiting toxicity in four of six patients treated at 150 mg sq/m. Assay of rubidazone in plasma samples obtained after administration of rubidazone showed that the drug was stable for at least 7 hr.

journal_name

Cancer Res

journal_title

Cancer research

authors

Kovach JS,Ames MM,Sternad ML,O'Connell MJ

subject

Has Abstract

pub_date

1979-03-01 00:00:00

pages

823-8

issue

3

eissn

0008-5472

issn

1538-7445

journal_volume

39

pub_type

杂志文章
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    authors: Rifkind AB,Tseng L,Hirsch MB,Lauersen NH

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    authors: Hehlmann R,Schetters H,Erfle V,Leib-Mösch C

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    authors: Yang G,Truong LD,Wheeler TM,Thompson TC

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    authors: Rabinovitch PS,Dziadon S,Brentnall TA,Emond MJ,Crispin DA,Haggitt RC,Bronner MP

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