The purpose of this research study is to show the blood pressure lowering effect of aprocitentan, a new drug, when added to the background antihypertensive therapy in patients with uncontrolled blood pressure and chronic kidney disease (CKD) stage 3 or 4. Participation in the research study will last up to 21 weeks (about 5 months).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Tablet, oral use once daily
Matching placebo tablet, oral use once daily
Change from Baseline to Week 4 of double-blind treatment in mean trough sitting systolic blood pressure measured by automated office blood pressure measurement.
Time frame: From baseline to Week 4 after treatment initiation
Change from baseline to Week 4 of double-blind treatment in mean trough sitting diastolic blood pressure measured by automated office blood pressure measurement.
Time frame: From baseline to Week 4 after treatment initiation
Ratio to baseline of urine albumin-to-creatinine ratio (UACR) at Week 4
Evaluated in the subgroup of participants with a UACR greater than 30 mg/g at baseline.
Time frame: From baseline to Week 4 after treatment initiation
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