Study to evaluate the safety and pharmacokinetics after co-administration of UIC201601 and UIC201602
- Conditions
- Endocrine, nutritional and metabolic diseases
- Registration Number
- KCT0007411
- Lead Sponsor
- Korea United Pharm
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Male
- Target Recruitment
- 40
1.Healthy male volunteers aged between 19 - 45 years at screening.
2.Subject who weight was = 55 kg and ideal body weight (IBW) was within ±20%
[IBW (kg) = (Height(cm) - 100) × 0.9]
3.Subject who don’t have congenital or chronic disease and any pathologic sign or symptom from medical check-up.
4.Subject who be within normal range by clinical laboratory results such as hematology test, blood chemistry test, urine test, etc.
5.Subject who be informed of and completely understood this clinical trial and signed the written informed consent for voluntary participation.
1.Subject who have a clinically significant past or present medical history of hepato-biliary, renal, respiratory, hematologic/neoplastic, urologic, psychiatric, cardiovascular (hypertension, angina, heart failure, myocardial infarction, etc.)and endocrine diseases(diabetes, hyperlipidemia).
2.Subject with a history of gastrointestinal disease (e.g. Crone’s disease, ulceration, acute or chronic pancreatitis, etc) or surgery (except simple appendectomy or repair of a hernia), which can influence the absorption of the study drug.
3.Subjects with hypersensitivity reactions to drugs like Atorvastatin, HMG-CoA reductase inhibitor.
4.Subjects with hypersensitivity reactions to drugs like Omega-3 or fish.
5.Uncontrolled genetic disorders such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.
6.Subject who was systolic blood pressure (SBP) = 140 mmHg mmHg or < 90 mmHg, diastolic blood pressure (DBP) = 95 mmHg or < 60 mmHg or pulse rate (PR) = 100 /min.
7.Subject who was HDL-cholesterol < 35 mg/dL.
8.Subject who persistent abnormalities in serum potassium concentration (<3.4 mEq/L or >5.5 mEq/L at screening visit).
9.Subjects who with a history of muscle disorders or hereditary muscle disorders or family history.
10.Subject with a biliary obstruction.
11.Subject with active liver disease with persistent and unexplained elevated serum transaminase or AST(GOT), ALT(GPT) > Upper reference rage limit x 3.
12.Subject with severe renal dysfunction(creatinine clearance with Cockroft-Gault < 30 mL/min).
13.Subject with a history of drug abuse.
14.Subject who took barbiturates or an inducer or inhibitor of drug metabolite enzymes or have consumed excessive alcohol within 1 month before the first study drug administration.
15.Subject who used ethical-the-counter drugs or herbal medicine within 2 weeks prior to the scheduled 1st study drug administration and who used over-the-counter drugs or vitamin within 10 days prior to the scheduled 1st study drug administration (But, subject whose other conditions are judged by investigators as appropriate for this clinical trial could participate in this study).
16.Subjects who has participated in any other clinical trial either for investigational or marketed drugs within 3 months prior to the scheduled 1st study drug administration.
17.Subject who donated whole blood within 2 months or blood components within 1 month before the first administration, or who received blood transfusion within 1 month before the first administration.
18.Subject who continuously drink alcohol (more than 21 units/week, 1 unit = 10 g of pure alcohol) or cannot abstain from alcohol from unable to refrain from drinking during within 24 hours prior to hospitalization and until discharge.
19.Smokers with an average daily smoking amount exceeding 10 cigarettes per day in recent 3 months.
20.Subject who have ingested or can not forcibly consume caffeine-containing foods (coffee, green tea, black tea, carbonated drink, coffee milk, nourishment drink, etc.) until discharge.
21.Subjects who were judged by investigator as inappropriate to participate in the clinical trial due to the results of clinical laboratory test results or other reasons
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Area under the plasma drug concentration-time curve within a dosing interval (t) at steady state;Minimum concentration of drug in plasma at steady state
- Secondary Outcome Measures
Name Time Method Minimum concentration of drug in plasma at steady state;Time of maximum concentration at steady state;Apparent Clearance at steady state