The objective of the study is to assess the pharmacodynamic properties of drug-drug of SHR4640 and Febuxostat interaction in patients with Hyperuricemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Tablet,dose1,QD
Tablet,dose2,QD
The Affiliated Hospital of QingDao University
Qingdao, Shandong, China
RECRUITINGPeak Plasma Concentration (Cmax) of SHR4640 and Febuxostat from plasma
Time frame: Day1 to Day 14
Area under the plasma concentration versus time curve (AUC) of SHR4640 and Febuxostat from plasma
Time frame: Day1 to Day 14
Apparent terminal half-life (t1/2) of SHR4640 and Febuxostat from plasma
Time frame: Day1 to Day 14
Number of Participants With Adverse Events (AEs) and Serious Adverse Events
Laboratory indicators, 12-lead electrocardiogram (ECG), physical examination,vital signs, adverse events (NCI-CTC AE 5.0), etc.
Time frame: Clinical significant changes from Day-21 up to Day 29
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