None listed
Conditions
Interventions
Drug : Reference drug: Lipitor 20mg 1 tablet + Lipidil supra 160mg 1 tablet
Test drug: CKD-337 1 capsule
Sponsors
Chong Kun Dang
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. Healthy male older than 19 years at the time of screening 2. BMI 17.5~30.5 kg/m2 and body weight more than 55kg 2. Subject who is no chronic disease, no symptoms or pathological findings 4. Suitable subject who is determined by laboratory tests(hematology test, blood chemistry, urinalysis test) according to the characteristics of the drug and ECG test at the time of screening 5. Subject who fully understand the clinical trials after in-depth explanation, decided to join the clinical trials by their will and signed inform consent
Exclusion criteria
Exclusion criteria: 1. Subject who has a history of hepatic, kidneys, neurological, respiratory, endocrine, hemato-oncology, urinary, cardiovascular, musculoskeletal or psychiatric diseases that is clinically significant and who has a following history 1) Gallbladder disease including cholelithiasis, severe hepatic impairment 2) Acute/chronic pancreatitis due to hypertriglyceridemia 3) Pulmonary embolism or interstitial lung disease 4) Genetic problems such as galactose intolerance, Lapp lactase deficiency, glucose-galactose malabsorption 5) Hypoalbuminemia 6) Alcoholics 7) Predisposition to rhabdomyolysis 2. Subject who has a history of gastrointestinal disease or gastrointestinal surgery which can affect drug absorption 3. Subject who has hypersensitivity to the drug composition containing choline fenofibrate, fenofibrate or atorvastatin, and other drug(aspirin, fenofibrate series, antibiotic and so on) 4. The following clinical significant findings at the time of screening * QTc > 450ms * PR interval > 200msec * QRS duration > 120msec 5. The following results in the clinical laboratory tests * CPK > 2 x upper limit of normal range * Liver function test (AST, ALT, ALP, Total bilirubin, ?-GT) > 2 x upper limit of normal range * eGFR(estimated GFR) < 60 mL/min/1.73m2 6. Systolic blood pressure = 160mmHg or = 100mmHg, Diastolic blood pressure = 95mmHg or = 60mmHg at the time of screening 7. History of drug abuse or a positive reaction for drug abuse at the screening test for urine 8. Taking ETC, oriental medicine within 2 weeks and OTC, vitamin within 1 week before the first dosing 9. Taking the medication involved in other clinical trials within 3 months before the first dosing 10. Whole blood donation with 2 months or component blood donation within 1 month or blood transfusion within 1 month before the first dosing 11. Alcohol > 21 units/week (1unit=10g of pure alcohol), within 6 month before the first dosing 12. Smoker(> 10 cigarettes/day) for the last 3 months 13. Comsumption of grapefruit of food containing grapefruit during clinical trial period from first dosing 48hours ago 14. Comsumption of food containing caffeine(e.g. coffee, green tea) during 24 hours ago IP dosing at discharge 15. Not using a reliable contraception, planning a pregnancy during the study 16. An impossible one who participates in clinical trial by investigator’s decision including laboratory test result
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| AUCt, Cmax of Atorvastatin ;AUCt, Cmax of Fenofibric acid | — |
Secondary
| Measure | Time frame |
|---|---|
| AUCinf, Tmax, t1/2, CL/F, Vd/F of Atorvastatin ;AUCinf, Tmax, t1/2, CL/F, Vd/F of Fenofibric acid;AUCt, Cmax, AUCinf, Tmax, t1/2, CL/F, Vd/F of 2-hydroxy atorvastatin | — |
Countries
Korea, Republic of
Contacts
Public ContactMin Kyu Park
Dong-A University Hospital
Outcome results
None listed