Healthy Male Subjects
Conditions
Keywords
amlodipine, valsartan, hypertension
Brief summary
To assess the pharmacokinetic characteristics of valsartan and S-amlodipine after single oral administration of Exforge tab. 10/160mg, a combination formulation of valsartan and amlodipine as reference drug and Lodivixx tab. 5/160mg, a combination formulation of valsartan and S-amlodipine as test drug in healthy male adults
Detailed description
The purpose of this study is to assess the pharmacokinetic characteristics of valsartan and S-amlodipine after single oral administration of Exforge tab. 10/160mg, a combination formulation of valsartan and amlodipine as reference drug and Lodivixx tab. 5/160mg, a combination formulation of valsartan and S-amlodipine as test drug in healthy male adults. Additionally the safety and tolerability of two drugs will be evaluated.
Interventions
Sponsors
Hanlim Pharm. Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
20 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Years 20-45 * Body weight ≥ 50kg and 18 ≤ BMI ≤ 29kg/m2 * Volunteer for the study and sign to ICF
Exclusion criteria
* Subject with serious active cardiovascular, respiratory, hepatologic, renal, hematologic, gastrointestinal, immunologic, dermal, neurologic, or psychological disease or history of such disease * Subject with symptoms of acute disease within 28 days prior to study medication * Subject with history which affect on the absorption, distribution, metabolism or excretion of drug * Subject with clinically significant active chronic disease * Subject with any of the following conditions in laboratory test i. AST(sGOT) or ALT(sGPT) \> Upper normal limit × 1.5 ii. Total bilirubin \> Upper normal limit × 1.5 iii. renal failure with Creatinine clearance \< 50mL/min * Clinically significant hypotension when screening period (SBP \< 100mmHg, DBP \< 60mmHg) * Positive test results for HBs Ab, HCV Ab, Syphilis regain test * Use of any prescription medication within 14 days prior to study medication * Use of any medication such as over-the-counter medication including oriental medication within 7 days prior to study medication dosing * Subject with clinically significant allergic disease (except for mild allergic rhinitis and mild allergic dermatitis that are not needed to administer drug) * Subject with known for hypersensitivity reaction to S-amlodipine, amlodipine and valsartan and dihydropyridine derivatives * Subject who is not able to taking the institutional standard meal * Subjects with whole blood donation within 60 days, component blood donation within 20 days * Subjects receiving blood transfusion within 30 days prior to study medication dosing * Participation in any clinical investigation within 60 days prior to study medication dosing * Continued excessive use of caffeine (caffeine \> five cups/day), severe heavy smoker (cigarette \> 10 cigarettes per day) and alcohol (alcohol\>30 g/day) * Subject who has been taken meal which affect on the absorption, distribution, metabolism, excretion of drug, especially grapefruit juice * Subject taking inducer or inhibitor of drug metabolism enzyme such as barbital within 28 days prior to study medication dosing * Continued serum potassium concentration abnormal status (on baseline visit, \< 3.5 mEq/L or \> 5.5 mEq/L) * Subjects with decision of nonparticipation through investigator's review due to laboratory test results or other excuse such as non-responding to request or instruction by investigator * Severe renal insufficient subjects (creatinine clearance : less than 10 mL/min) * Severe hepatic insufficient subjects,billiary cirrhosis, biliary obstruction and cholestasis patient * Combination with aliskiren in Diabetic patient or moderate to severe renal insufficient subjects (glomerular filtration rate\<60 mL/min/1.73m2)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cmax (maximum concentration) | 0 hour, 1 hour, 1.5 hour, 2 hour, 2.5 hour, 3 hour, 3.5 hour, 4 hour, 4.5 hour, 5 hour, 6 hour, 8 hour, 12 hour, 24 hour, 48 hour, 72 hour |
| AUC(area under curve) | 0 hour, 1 hour, 1.5 hour, 2 hour, 2.5 hour, 3 hour, 3.5 hour, 4 hour, 4.5 hour, 5 hour, 6 hour, 8 hour, 12 hour, 24 hour, 48 hour, 72 hour |
Secondary
| Measure | Time frame |
|---|---|
| Number of participants with adverse events | 0 hour, 1 hour, 1.5 hour, 2 hour, 2.5 hour, 3 hour, 3.5 hour, 4 hour, 4.5 hour, 5 hour, 6 hour, 8 hour, 12 hour, 24 hour, 48 hour, 72 hour |
Outcome results
None listed