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    Article

    Disposition of 9-nitrocamptothecin and its 9-aminocamptothecin metabolite in relation to ABC transporter genotypes

    Purpose: The source of the pharmacokinetic variability of 9-nitrocamptothecin (9NC) and its 9-aminocamptothecin (9AC) metabolite is unknown. ATP-binding cassette (ABC) transporters have been reported to modulate ...

    William C. Zamboni, Ramesh K. Ramanathan, Howard L. McLeod in Investigational New Drugs (2006)

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    Article

    Clinical and pharmacokinetic study evaluating the effect of food on the disposition of 9-nitrocamptothecin and its 9-aminocamptothecin metabolite in patients with solid tumors

    Background: 9-Nitrocamptothecin (9NC) is an orally administered camptothecin analogue that has completed phase III trials for pancreatic cancer. In biological matrices, camptothecin analogues exist in equilibrium...

    William C. Zamboni, Sanjay Goel, Tahir Iqbal in Cancer Chemotherapy and Pharmacology (2006)

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    Phase I and pharmacokinetic study of the novel redox-active agent, motexafin gadolinium, with concurrent radiation therapy in patients with locally advanced pancreatic or biliary cancers

    Purpose: To determine the maximum tolerated dose and dose-limiting toxicity (DLT) of the novel anticancer agent, motexafin gadolinium (MGd), administered concurrently with radiation thera...

    Ramesh K. Ramanathan, Marwan Fakih, Sridhar Mani in Cancer Chemotherapy and Pharmacology (2006)

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    Article

    Biliary excretion of 17-(allylamino)-17-demethoxygeldanamycin (NSC 330507) and metabolites by Fischer 344 rats

    17-(Allylamino)-17-demethoxygeldanamycin (17AAG), an analogue of the benzoquinone ansamycin geldanamycin, has been extensively studied preclinically and is being evaluated clinically. Studies were performed to...

    Steven M. Musser, Merrill J. Egorin in Cancer Chemotherapy and Pharmacology (2003)

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    Article

    Pharmacokinetics and tissue distribution of halofuginone (NSC 713205) in CD2F1 mice and Fischer 344 rats

    Purpose: Halofuginone (HF) inhibits synthesis of collagen type I and matrix metalloproteinase-2 and is being considered for clinical evaluation as an antineoplastic agent. Pharmacokinetic studies...

    Kataleeya P. Stecklair, Deborah R. Hamburger in Cancer Chemotherapy and Pharmacology (2001)

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