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- W2081571728 abstract "Objective: To evaluate the absorption, metabolism, and excretion of tivozanib, a new investigational drug for renal cell carcinoma and solid malignancies. Methods: Eight healthy male participants received a single 1.5-mg (˜160 μCi) dose of oral [14C]-tivozanib. Whole blood, serum, urine, and feces were evaluated up to 28 days postdose for pharmacokinetics, radioanalysis, and metabolites. Adverse events were recorded throughout the study. Results: [14C]-tivozanib concentration peaked at 10.9 ± 5.84 hours. The mean serum half-life for [14C]-tivozanib was 89.3 ± 23.5 hours. The maximum concentration and area under the curve for [14C]-tivozanib were 12.1 ± 5.67 ng/mL and 1084 ± 417.0 ng·h/mL, respectively. Mean recovery of total radioactivity was 91.0% ± 11.0%; 79.3% ± 8.82% of the radioactivity was recovered in feces both as unchanged tivozanib and metabolites. In the urine, 11.8% ± 4.59% was recovered only as metabolites. No unchanged tivozanib was found in the urine. Conclusion: Tivozanib had a long half-life with no major circulating metabolite, was well tolerated as a single dose, and was primarily eliminated via feces with no unchanged tivozanib found in urine. These pharmacokinetic data of [14C]-tivozanib are consistent with previous studies of unlabeled tivozanib." @default.
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- W2081571728 date "2012-06-28" @default.
- W2081571728 modified "2023-09-26" @default.
- W2081571728 title "Absorption, Metabolism, and Excretion of [14C]-Tivozanib, a Vascular Endothelial Growth Factor Receptor Tyrosine Kinase Inhibitor, in Healthy Male Participants: A Phase I, Open-Label, Mass-Balance Study" @default.
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- W2081571728 doi "https://doi.org/10.1177/2160763x12447303" @default.
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