Pharmacokinetic Drug Interaction Between Rosuvastatin and Valsartan
A Randomized, Open-label, Multiple-dose, Crossover Study to Investigate the Pharmacokinetic Drug Interaction Between Rosuvastatin and Valsartan in Healthy Male Volunteer
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 1
Contacts and Locations
Study Locations
-
-
-
Seoul, Korea, Republic of
- Yuhan Corporation
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Healthy male volunteers of aged between 20 years to 50 years
- Have a body mass index (BMI) between 19kg/m2 and 27kg/m2 inclusive
- Eligible subjects with acceptable medical history, physical examination laboratory tests, ECG during screening period
- Able to follow instruction and can participate in whole procedure of the trial
- Have signed a written informed consent voluntary, prior to the any procedure, using a form that is approved by the local Institutional Review Board after detail explanation of the drug
- Anticipate having the same adult female sexual partner, who have no possibility of being pregnant or breast-feeding and take steps to prevent conception during the study
Exclusion Criteria:
- Have history of cardiovascular disorder(congestive heart failure, complications of coronary artery stenosis stroke and etc.), respiratory disorder, renal disorder(severe renal failure and etc.), liver disorder(moderate or severe liver failure and etc.) endocrine system disorder(diabetics, impaired glucose tolerance and etc.), digestive system disorder, central nervous system disorder, mental illness or malignant tumor
- Have history of gastrointestinal disease(Crohn's disease, ulcer and etc.), gastrointestinal surgery(simple appendectomy or herniotomy excluded) that can affect the absorption of the drug
- Have suffered from a clinically significant disease within 30 days prior to the first administration
- Have a known hypersensitivity or history of clinically significant hypersensitivity to drugs including the same class drugs with rosuvastatin or valsartan, or other drug(aspirin, antibiotics and etc.)
- Have genetic myopathy, family history of myopathy, or history of myopathy to drugs
- Have systolic blood pressure higher than 150mmHg or lower than 90mmHg, or diastolic blood pressure higher than 100mmHg or lower than 60mmHg, or pulse rate more than 100times/min or less than 40times/min
- Have history of drug abuse or shown positive on drug abuse during drug screening test
- Participated in any other clinical trials within 90 days prior to the first administration
- Have used any herbal medicine, prescription drug, or generic medicine within 30 days, 14 days or 7 days prior to the first administration, respectively (provided, however, if other conditions are judged to be eligible by investigators, subjects can participate in the trial)
- Donated whole blood or blood component within 60 days or 30 days prior to the first administration, respectively, or received transfusion within 30 days prior to the first administration
- Excessive alcohol drinker(> 140g/week; 1 glass of 12° wine(125mL) = 12.0g, 1 glass of 4° beer(250mL) = 8g, 0.5 bottle of soju(180mL) = 28.8g)
- Heavy smoker(> 20 cigarettes/day)
- Excessive caffeine drinker(> 4 cups/day)
- Shown positive on serum test(HBsAg, HCV Ab, HIV Ab tests)
- Subject who is judged to be ineligible by principal investigator or sub-investigator according to various reasons including their abnormal values in clinical laboratory test
- Continuous increase of liver enzyme level(AST, ALT) of unknown cause or active liver disorder patients with liver enzyme level increasing more than 3 time of normal upper limit
- Severe renal disorder patients(with creatinine clearance (Cr) < 10mL/min when calculated with Modification of Diet in Renal Disease method)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: CROSSOVER
- Masking: NONE
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
EXPERIMENTAL: Sequence 1
|
Period 1(A) Period 2(B) Period 3(C) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
|
EXPERIMENTAL: Sequence 2
|
Period 1(C) Period 2(A) Period 3(B) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
|
EXPERIMENTAL: Sequence 3
|
Period 1(B) Period 2(C) Period 3(A) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
|
EXPERIMENTAL: Sequence 4
|
Period 1(C) Period 2(B) Period 3(A) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
|
EXPERIMENTAL: Sequence 5
|
Period 1(B) Period 2(A) Period 3(C) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
|
EXPERIMENTAL: Sequence 6
|
Period 1(A) Period 2(C) Period 3(B) A: Rosuvastatin 20mg (once daily for 4 consecutive days), B: Valsartan 160mg (once daily for 4 consecutive days), C: Rosuvastatin 20mg plus Valsartan 160mg (once daily for 4 consecutive days)
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Cmax,ss of valsartan
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
AUCt,ss of valsartan
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Cmax,ss of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
AUCt,ss of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
t1/2 of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
t1/2 of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Tmax,ss of valsartan
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
t1/2 of valsartan
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Cmin,ss of valsartan
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Tmax,ss of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Cmin,ss of rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
Cmax,ss of N-desmetyl rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
|
AUCt,ss of N-desmetyl rosuvastatin
Time Frame: 18 points up to Day 4
|
18 points up to Day 4
|
Collaborators and Investigators
Sponsor
Sponsor
Investigators
Investigators
- Principal Investigator: Woo-Seung Huh, MD, PhD., Samsung Medical Center
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (ACTUAL)
Primary Completion
Study Completion (ACTUAL)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
First Posted
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Metabolic Diseases
- Lipid Metabolism Disorders
- Dyslipidemias
- Hyperlipidemias
- Molecular Mechanisms of Pharmacological Action
- Antihypertensive Agents
- Enzyme Inhibitors
- Antimetabolites
- Anticholesteremic Agents
- Hypolipidemic Agents
- Lipid Regulating Agents
- Hydroxymethylglutaryl-CoA Reductase Inhibitors
- Angiotensin II Type 1 Receptor Blockers
- Angiotensin Receptor Antagonists
- Valsartan
- Rosuvastatin Calcium
Other Study ID Numbers
Other Study ID Numbers
- YH14700-101
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