To investigate the safety and pharmacokinetic properties of CJ-30039 and Lipidil Supra
Study objectives * To compare the safety and pharmacokinetic properties of CJ-30039 and Lipidil Supra after a single oral administration in healthy male volunteers. * To evaluate the food-effect on pharmacokinetics of CJ-30039 after a single oral administration in healthy male volunteers.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
48
single dose
single dose
Yonsei university severance hospital
Seoul, South Korea
Peak Plasma Concentration (Cmax) of fenofibric acid
Time frame: up to 48 hours
Area under the plasma concentration versus time curve (AUC) of fenofibric acid
Time frame: up to 48 hours
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