The purpose of this study is to evaluate the effect of ION904 on plasma angiotensinogen (AGT) in participants with uncontrolled hypertension.
This is a Phase 2, multicenter, double-blind, randomized, placebo-controlled study. It will include up to approximately 48 participants with mild to moderate hypertension who have uncontrolled blood pressure (˃ 130 - ≤ 170 millimeters of mercury \[mmHg\] systolic) and have been on one or more anti-hypertensive medications for at least one month. Following an up to 4-week screening period, eligible participants will receive multiple doses of ION904 during a 13-week treatment period, followed by a 13-week post-treatment follow-up period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
48
Altasciences - Los Angeles
Cypress, California, United States
National Research Institute
Los Angeles, California, United States
Clinical Trials Research
Sacramento, California, United States
ALL Medical Research, LLC
Cooper City, Florida, United States
Percent Change from Baseline in Plasma Angiotensinogen (AGT)
Time frame: Baseline up to approximately 15 weeks
Change from Baseline in Seated Automated Office Systolic Blood Pressure (SBP)
Time frame: Baseline up to approximately 15 weeks
Change from Baseline in Seated Automated Office Diastolic Blood Pressure (DBP)
Time frame: Baseline up to approximately 15 weeks
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Port Orange, Florida, United States
Altasciences
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NY Scientific
Brooklyn, New York, United States
Juno Research, LLC
Houston, Texas, United States