The primary purpose of this study is to investigate potential pharmacokinetic interaction in healthy volunteers when apatinib is administered in combination with rifampicin. Secondary objective is evaluating the safety and tolerability of apatinib alone and when co-administered with rifampicin.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
apatinib was administered in the morning after an overnight fast of at least 10 h
rifampicin was administered in the morning 2 hours after breakfast
Shanghai Xuhui Central Hospital
Shanghai, Shanghai Municipality, China
Area under the plasma concentration versus time curve (AUC) of Apatinib
Time frame: 0~72h after apatinib administration
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time frame: From first administration to the seventh day after last administration
Peak Plasma Concentration (Cmax) of Apatinib
Time frame: 0~72h after apatinib administration
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