The purpose of this study is to evaluate of efficacy and safety of HCP1904-1 and RLD2001-1 alone in patients with essential hypertension inadequately controlled on RLD2001-1 monotherapy.
A Multi-center, Randomized, Double-blinded, Active-controlled, Parallel, Phse III Study to Evaluate the Efficacy and Safety of HCP1904-1 in Essential Hypertension Patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
123
Severance Hospital
Seoul, South Korea
Change from baseline in mean sitting systolic blood pressure(mmHg)
Time frame: Week 8
Change from baseline in mean sitting systolic blood pressure(mmHg)
Time frame: Week 4
Change from baseline in mean sitting diastolic blood pressure(mmHg)
Time frame: Week 4,8
Change from baseline in mean pulse blood pressure(mmHg)
Time frame: Week 4,8
Responder rate
Time frame: Week 4, 8
target blood pressure reach rate
Time frame: Week 4, 8
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