Clinical Trial to Evaluate the Efficacy and Safety of D064 and D702 Combination Therapy
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
346
Experimental Group Subjects assigned to this group are treated with D064, D702, placebo of D660
Experimental Group Subjects assigned to this group are treated with D660, placebo of D064, placebo of D702
Seoul National University Bundang Hospital
Seongnam, Bundang-gu, South Korea
Change from baseline in MSSBP
MSSBP(Mean Sitting Systolic Blood Pressure)
Time frame: 8 weeks after drug administrations
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