Literature DB >> 3865774

Phase I clinical evaluation of oral and intravenous 4-demethoxydaunorubicin.

J J Kavanagh, K Y Yeung, N Savaraj, I H Krakoff.   

Abstract

Thirteen patients were treated with both the oral and intravenous preparations of 4-demethoxydaunorubicin (DMDR). The drug was well tolerated in both forms. Neutropenia was the dose-limiting side-effect. Approximately 30% of the compound was absorbed when given orally. The maximum tolerated dose was 12.5 mg/m2 intravenously or 50 mg/m2 (10 mg/m2 q d X 5) orally, given every 21-28 days.

Entities:  

Mesh:

Substances:

Year:  1985        PMID: 3865774     DOI: 10.1016/0277-5379(85)90013-6

Source DB:  PubMed          Journal:  Eur J Cancer Clin Oncol        ISSN: 0277-5379


  1 in total

1.  A phase II study of oral idarubicin (4-demethoxydaunorubicin) in advanced breast cancer.

Authors:  N S Stuart; M H Cullen; T J Priestman; G R Blackledge; C J Tyrrell
Journal:  Cancer Chemother Pharmacol       Date:  1988       Impact factor: 3.333

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.