Search Results - "Vernillet, L."
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Multicentre phase II study and pharmacokinetic analysis of irinotecan in chemotherapy-naive patients with glioblastoma
Published in Annals of oncology (01-04-2003)“…To assess the antitumour activity and safety profile of irinotecan and its pharmacokinetic interactions with anticonvulsants in patients with glioblastoma…”
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Phase I Dose-Finding Study of a New Taxane, RPR 109881A, Administered as a One-Hour Intravenous Infusion Days 1 and 8 to Patients With Advanced Solid Tumors
Published in Journal of clinical oncology (15-12-2000)“…To define the maximum-tolerated dose, recommended phase II dose (RD), dose-limiting toxicity (DLT), and pharmacokinetics of a novel taxane, RPR 109881A,…”
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Effect of food or antacid on febuxostat pharmacokinetics and pharmacodynamics in healthy subjects
Published in Clinical pharmacology and therapeutics (01-02-2005)“…Febuxostat is a novel non‐purine selective inhibitor of xanthine oxidase (NP‐SIXO) being developed for the management of hyperuricemia in patients with gout…”
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Effects of age and gender on febuxostat pharmacokinetics, pharmacodynamics, and safety in healthy subjects
Published in Clinical pharmacology and therapeutics (01-02-2005)“…Background Febuxostat is a novel non‐purine selective inhibitor of xanthine oxidase (NP‐SIXO) being developed for the management of hyperuricemia in patients…”
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Effect of febuxostat on pharmacokinetics of desipramine, a CYP2D6 substrate, in healthy subjects
Published in Clinical pharmacology and therapeutics (01-02-2005)“…Febuxostat is a novel non‐purine selective inhibitor of xanthine oxidase (NP‐SIXO) being developed for the management of hyperuricemia in patients with gout…”
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Docetaxel in combination with 5-fluorouracil in patients with metastatic breast cancer previously treated with anthracycline-based chemotherapy: a phase I, dose-finding study
Published in European journal of cancer (1990) (01-09-2000)“…This phase I study evaluated the maximum tolerated dose, dose-limiting toxicity and recommended dose of docetaxel in combination with 5-fluorouracil (5-FU) in…”
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Phase I study of irinotecan and raltitrexed in patients with advanced gastrointestinal tract adenocarcinoma
Published in British journal of cancer (01-07-2000)“…To determine the dose-limiting toxicities (DLT) and maximum tolerated dose (MTD) of irinotecan and raltitrexed given as sequential short infusions every 3…”
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Phase I dose-finding and pharmacokinetic study of docetaxel and vinorelbine as first-line chemotherapy for metastatic breast cancer
Published in Annals of oncology (01-07-2001)“…Background and purpose: Anthracycline-containing regimens are widely used in advanced breast cancer. However, there is a need for new, non-anthracycline…”
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Phase I study of docetaxel in combination with cyclophosphamide as first-line chemotherapy for metastatic breast cancer
Published in British journal of cancer (04-11-2002)“…This phase I was study conducted to establish the maximum tolerated dose, dose-limiting toxicity, and recommended dose of docetaxel in combination with…”
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A rapid reversed phase high performance liquid chromatographic method for the determination of docetaxel (Taxotere®) in human plasma using a column switching technique
Published in Journal of pharmaceutical and biomedical analysis (01-09-1998)“…A rapid, simple and sensitive isocratic high performance liquid chromatography (HPLC) method was developed to measure the concentration of docetaxel in plasma…”
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Noninterchangeability of specific radioimmunoassay and monoclonal antibody fluorescent polarization immunoassay in cyclosporine measurements
Published in Fundamental & clinical pharmacology (01-01-1996)“…This study compares cyclosporine (CsA) concentrations in whole blood from patients receiving bone marrow (n = 10), renal (n = 48), heart (n = 50) or liver (n =…”
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Pharmacokinetics and pharmacodynamics of febuxostat, a new non-purine selective inhibitor of xanthine oxidase in subjects with renal impairment
Published in American journal of therapeutics (01-01-2005)“…To assess the safety, pharmacokinetics, and pharmacodynamics of febuxostat in subjects with normal renal function or renal impairment, febuxostat (80 mg/d) was…”
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Metabolism of Irinotecan (CPT-11) by CYP3A4 and CYP3A5 in Humans
Published in Clinical cancer research (01-05-2000)“…7-Ethyl-10[4-(1-piperidino)-1-piperidino] carbonyloxycamptothecin (CPT-11), a DNA topoisomerase I inhibitor, undergoes several metabolic pathways to generate…”
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Monoclonal antibodies for radioimmunoassay of cyclosporine: a multicenter comparison of their performance with the Sandoz polyclonal radioimmunoassay kit
Published in Clinical chemistry (Baltimore, Md.) (01-06-1988)“…The performance of a radioimmunoassay kit containing monoclonal specific and nonspecific antibodies to cyclosporine (Sandimmun-Kit; Sandoz Ltd., Basle,…”
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The Effect of Mild and Moderate Hepatic Impairment on Pharmacokinetics, Pharmacodynamics, and Safety of Febuxostat, a Novel Nonpurine Selective Inhibitor of Xanthine Oxidase
Published in Journal of clinical pharmacology (01-01-2006)“…To assess the effect of hepatic impairment on the pharmacokinetics, pharmacodynamics, and safety of febuxostat at steady state, multiple once‐daily 80‐mg oral…”
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Influence of different parameters for the monitoring of cyclosporine
Published in Transplantation proceedings (01-06-1990)Get more information
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Dosage Adjustment and Pharmacokinetic Profile of Irinotecan in Cancer Patients With Hepatic Dysfunction
Published in Journal of clinical oncology (01-11-2002)“…To determine the recommended dose (RD) and the pharmacokinetic profile of irinotecan and its metabolites in cancer patients with hyperbilirubinemia. Patients…”
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Metabolism of irinotecan (CPT-11) by human hepatic microsomes : Participation of cytochrome P-450 3A and drug interactions
Published in Cancer research (Chicago, Ill.) (01-02-1998)“…Irinotecan (CPT-11) is a water-soluble analogue of camptothecin showing activity in colon cancer. Recently, we identified a major metabolite of CPT-11 in…”
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