The objective of this clinical study is to evaluate the efficacy and safety by comparing BR1017A+BR1017B treatment group to BR1017A treatment group and BR1017B treatment group respectively at Week 8 in essential hypertension patients with primary hypercholesterolemia
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
148
Subjects take the investigational products once a day for 8 weeks.
Subjects take the investigational products once a day for 8 weeks.
Subjects take the investigational products once a day for 8 weeks.
Severance Hospital
Seoul, South Korea
Mean sitting systolic blood pressure
The change of mean sitting systolic blood pressure from baseline in BR1017A+BR1017B at Week 8 compared to BR1017B
Time frame: 8weeks from Baseline Visit
LDL-C
The percent of change in LDL-C from baseline in BR1017A+BR1017B at Week 8 compared to BR1017A
Time frame: 8weeks from Baseline Visit
LDL-C
The percent of change in LDL-C from baseline in BR1017A+BR1017B at Week 8 compared to BR1017B
Time frame: 8weeks from Baseline Visit
Mean sitting systolic blood pressure
The change of mean sitting systolic blood pressure from baseline in BR1017A+BR1017B at Week 8 compared to BR1017A
Time frame: 8weeks from Baseline Visit
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Subjects take the investigational products once a day for 8 weeks.