The bioequivalence study of Capecitabine in Patients with Breast or Colorectal Cancer under Fed condition
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下载链接：
https://www.omicsdi.org/dataset/ecrin-mdr-crc/2575050
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资源简介：
Intervention1: Capecitabine: 1250 mg/m2 oral twice a day for one day
Control Intervention1: Xeloda: 1250 mg/m2 oral twice a day for two days
Primary outcome(s): Pharmacokinetic parameters: Cmax and AUC0-t of capecitabine in plasma.Timepoint: 0.250, 0.500, 1.000, 1.500
Study Design: Randomized, Crossover Trial
Method of generating randomization sequence:Other Method of allocation concealment:Other Blinding and masking:Open Label
创建时间：
2013-11-15
