The purpose of this study is to evaluate the safety and efficacy of fixed combination of amlodipine(5mg or 10mg) and losartan (50 mg or 100 mg), amlodipine and losartan alone in reducing blood pressure. The study will investigate the dose response relationship for the combinations and monotherapies.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
320
amlodipine/losartan 5/50mg, 5/100mg, 10/50mg, 10/100mg
amlodipine 5mg, 10mg
Losartan 50mg, 100mg
14 sites in Korea
Seoul, Busan, Etc., South Korea
Average changes from baseline in sitDBP
Time frame: Week 8
Average changes from baseline in sitDBP
Time frame: Week 4
Average changes from baseline in sitSBP
Time frame: Week 4, 8
Blood pressure responder rate
Time frame: Week 4, 8
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