The purpose of this study is to evaluate of efficacy and safety of HCP1904-3 and RLD2001-1 alone in patients with essential hypertension inadequately controlled on RLD2001-1 monotherapy.
A Multi-center, Randomized, Double-blinded, Active-Controlled, Parallel, Phase III Study to Evaluate the Efficacy and Safety of HCP1904-3 in Essential Hypertension patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
166
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
Target blood pressure reach rate(%)
Time frame: Week 4,8
Blood pressure responder rate(%)
Time frame: Week 4,8
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