Hypertension
Conditions
Keywords
Hypertension, Hypertensive, AGT, Angiotensinogen, Blood Pressure
Brief summary
The purpose of this study was to evaluate the effect of IONIS-AGT-LRx compared to placebo on seated automated office systolic blood pressure (SBP) from baseline to Study Day 85 in uncontrolled hypertensive participants on ≥ 3 antihypertensive medications and to evaluate the effect of IONIS-AGT-LRx on ambulatory blood pressure, seated automated office SBP, seated automated office diastolic blood pressure (DBP), and plasma angiotensinogen (AGT) at each scheduled visit in uncontrolled hypertensive participants on ≥ 3 antihypertensive medications.
Detailed description
This was a phase 2, double-blind, randomized, placebo-controlled study in up to 160 participants. Participants were randomized in a 2:1 ratio and received a once-weekly subcutaneous (SC) treatment with either IONIS-AGT-LRx or matching placebo. The length of participation in the study was approximately 31 weeks, which included an up to 6-week screening period, a 12-week treatment period, and a 13-week post-treatment period.
Interventions
ISIS 757456 matching placebo administered by SC injection.
IONIS-AGT-LRx administered by SC injection.
Sponsors
Study design
Eligibility
Inclusion criteria
* Males or females aged 18-80 inclusive and weighing ≥ 50 kilograms (kg) at the time of informed consent * Females: must be non-pregnant and non-lactating, and either surgically sterile or post-menopausal * Males must be abstinent, surgically sterile or if engaged in sexual relations with a woman of childbearing potential (WOCBP), a highly effective contraceptive method must be used * Body mass index (BMI) ≤ 45.0 kilograms per square meter (kg/m\^2) * At screening, the participant must have been on a stable, maximally tolerated regimen (per Investigator judgement) of 3 or more antihypertensive medications for at least 1 month prior to screening and will be required to maintain this regimen throughout the study. The combination of antihypertensive medications must be in the following categories: a) angiotensin-converting enzyme inhibitor (ACEi) or angiotensin II receptor blocker (ARB), b) beta blocker: c) calcium channel blocker d) diuretic, e) alpha-1 blocker f) centrally acting sympatholytic agent or g) direct acting vasodilators (e.g. hydralazine)
Exclusion criteria
* Clinically significant abnormalities in screening laboratory results, medical history according to Investigator judgment * History of secondary hypertension (HTN) including, but not limited to any of the following: renovascular HTN (unilateral or bilateral renal artery stenosis), coarctation of the aorta, primary hyperaldosteronism, Cushing's disease, pheochromocytoma, polycystic kidney disease, and drug-induced HTN * The use of the following at time of screening and during the course of the study: * Other medications for the treatment of HTN (e.g., minoxidil, diazoxide, renin inhibitors) * Medications that may cause hyperkalemia unless on a stable dose at least 1 month prior to the screening visit and no known history of hyperkalemia per Investigator judgement * Use of oral anticoagulants, unless stable for 4 weeks prior to the first dose of study drug and regular monitoring must be performed per clinical practice during the study unless the participant is receiving vitamin K agonists. If the participant is receiving vitamin K antagonists (e.g., warfarin) international normalized ratio (INR) should be in therapeutic range, as established by the Investigator, for 4 weeks prior to the first dose * Chronic administration of non-steroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase 2 (COX-2) inhibitors (except aspirin for cardiovascular disease provided the total daily dose does not exceed 325 mg) * History of bleeding diathesis, coagulopathy, immune thrombocytopenic purpura (ITP), thrombotic cytopenic purpura (TTP), or any qualitative or quantitative platelet defect * Unstable/underlying known cardiovascular disease defined as: * Any history of congestive heart failure (New York Heart Association \[NYHA\] Class III-IV) * Any history of previous myocardial infarction, coronary revascularization, unstable or stable angina pectoris ˂ 1 year prior to screening * Any hemodynamically unstable atrial or ventricular arrhythmias * Significant uncorrected valvular heart disease * Any history of stroke or transient ischemic attack \< 1 year prior to screening * A cardiac valve repair, cardiac device implantation, and/or a hospitalization for heart failure within 3 months of screening * Participant works nighttime shifts (e.g., 11 PM to 7 AM)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change From Baseline in Seated Automated Office SBP to Day 85 | Baseline to Day 85 |
Secondary
| Measure | Time frame |
|---|---|
| Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169 |
| Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169 |
| Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Baseline, Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169 |
| Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Baseline, Day 85 |
| Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169 |
| Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Baseline, Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169 |
| Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Baseline, Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169 |
| Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Baseline, Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169 |
Countries
Canada, United States
Participant flow
Recruitment details
Participants took part in the study at investigative sites in the US and Canada from 28 April 2021 to 03 October 2022.
Pre-assignment details
Participants with uncontrolled hypertension who were on ≥ 3 antihypertensive medications were enrolled and randomized to receive either ISIS 757456 80 mg, ISIS 757456 120 mg or ISIS 757456 matched placebo for a 12-week treatment period.
Participants by arm
| Arm | Count |
|---|---|
| Pooled Placebo Participants received ISIS 757456 matching placebo, SC injection, once weekly for 12 weeks. | 53 |
| IONIS-AGT-LRx 80 mg Participants received ISIS 757456 80mg, SC injection, once weekly for 12 weeks. | 54 |
| IONIS-AGT-LRx 120 mg Participants received ISIS 757456 120 mg, SC injection, once weekly for 12 weeks. | 53 |
| Total | 160 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 | FG002 |
|---|---|---|---|---|
| Overall Study | Adverse Event or Serious Adverse Event (SAE) | 0 | 0 | 1 |
| Overall Study | Reason Not Specified | 1 | 3 | 3 |
| Overall Study | Voluntary Withdrawal | 4 | 1 | 2 |
Baseline characteristics
| Characteristic | Pooled Placebo | IONIS-AGT-LRx 80 mg | IONIS-AGT-LRx 120 mg | Total |
|---|---|---|---|---|
| Age, Continuous | 63.1 years STANDARD_DEVIATION 8.29 | 64.0 years STANDARD_DEVIATION 7.47 | 61.3 years STANDARD_DEVIATION 9.17 | 62.8 years STANDARD_DEVIATION 8.36 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 20 Participants | 15 Participants | 14 Participants | 49 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 33 Participants | 39 Participants | 39 Participants | 111 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Race/Ethnicity, Customized Race Asian | 0 Participants | 1 Participants | 2 Participants | 3 Participants |
| Race/Ethnicity, Customized Race Black | 16 Participants | 20 Participants | 21 Participants | 57 Participants |
| Race/Ethnicity, Customized Race Multiple Races | 0 Participants | 3 Participants | 0 Participants | 3 Participants |
| Race/Ethnicity, Customized Race Native Hawaiian or Other Pacific Islander | 1 Participants | 0 Participants | 1 Participants | 2 Participants |
| Race/Ethnicity, Customized Race Other Race | 1 Participants | 0 Participants | 0 Participants | 1 Participants |
| Race/Ethnicity, Customized Race White | 35 Participants | 30 Participants | 29 Participants | 94 Participants |
| Seated Automated Office Diastolic Blood Pressure (DBP) -FAS | 82.1 mmHg STANDARD_DEVIATION 8.91 | 81.5 mmHg STANDARD_DEVIATION 10.2 | 82.8 mmHg STANDARD_DEVIATION 10.32 | 82.1 mmHg STANDARD_DEVIATION 9.78 |
| Seated Automated Office Diastolic Blood Pressure (DBP)- PPS | 82.5 mmHg STANDARD_DEVIATION 8.5 | 80.6 mmHg STANDARD_DEVIATION 10.18 | 81.7 mmHg STANDARD_DEVIATION 10.48 | 81.6 mmHg STANDARD_DEVIATION 9.72 |
| Seated Automated Office Systolic Blood Pressure (SBP) -FAS | 147.6 mmHg STANDARD_DEVIATION 13.92 | 143.6 mmHg STANDARD_DEVIATION 10.04 | 144.1 mmHg STANDARD_DEVIATION 11.42 | 145.1 mmHg STANDARD_DEVIATION 11.95 |
| Seated Automated Office Systolic Blood Pressure (SBP)- PPS | 148.8 millimeters of mercury (mmHg) STANDARD_DEVIATION 12.51 | 143.3 millimeters of mercury (mmHg) STANDARD_DEVIATION 10.29 | 144.0 millimeters of mercury (mmHg) STANDARD_DEVIATION 11.35 | 145.3 millimeters of mercury (mmHg) STANDARD_DEVIATION 11.59 |
| Sex: Female, Male Female | 33 Participants | 32 Participants | 32 Participants | 97 Participants |
| Sex: Female, Male Male | 20 Participants | 22 Participants | 21 Participants | 63 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 53 | 0 / 54 | 1 / 53 |
| other Total, other adverse events | 9 / 53 | 18 / 54 | 14 / 53 |
| serious Total, serious adverse events | 1 / 53 | 2 / 54 | 1 / 53 |
Outcome results
Change From Baseline in Seated Automated Office SBP to Day 85
Time frame: Baseline to Day 85
Population: PPS included all FAS participants who received at least 10 of the 12 doses of study drug, did not alter antihypertensive medications during the treatment period and prior to Day 85, and had no significant protocol deviations that would have been expected to affect efficacy assessment.
| Arm | Measure | Value (LEAST_SQUARES_MEAN) |
|---|---|---|
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Day 85 | -9 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Day 85 | -13 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Day 85 | -9 mmHg |
Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit
Time frame: Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of the 12 doses of study drug, did not alter antihypertensive medications during the Treatment Period and prior to Study Day 85, and have no significant protocol deviations that would be expected to affect efficacy assessment. 'Number analyzed' indicates the number of participants with data available for analysis at the specified time point.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 106 | 756.89 nmol/L | Standard Deviation 212.891 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 120 | 746.63 nmol/L | Standard Deviation 190.789 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 148 | 753.35 nmol/L | Standard Deviation 186.906 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 43 | 837.24 nmol/L | Standard Deviation 251.61 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 169 | 797.92 nmol/L | Standard Deviation 238.442 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 15 | 878.36 nmol/L | Standard Deviation 239.895 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 57 | 848.45 nmol/L | Standard Deviation 256.088 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 71 | 790.50 nmol/L | Standard Deviation 256.568 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 85 | 793.77 nmol/L | Standard Deviation 202.796 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 92 | 748.11 nmol/L | Standard Deviation 204.231 |
| Pooled Placebo | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 29 | 836.74 nmol/L | Standard Deviation 228.202 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 71 | 308.99 nmol/L | Standard Deviation 174.893 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 29 | 388.61 nmol/L | Standard Deviation 193.723 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 92 | 330.68 nmol/L | Standard Deviation 176.868 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 120 | 531.33 nmol/L | Standard Deviation 203.681 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 85 | 328.28 nmol/L | Standard Deviation 199.364 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 57 | 303.03 nmol/L | Standard Deviation 168.53 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 148 | 658.33 nmol/L | Standard Deviation 248.413 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 15 | 575.68 nmol/L | Standard Deviation 248.708 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 106 | 429.04 nmol/L | Standard Deviation 175.316 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 169 | 676.60 nmol/L | Standard Deviation 236.881 |
| IONIS-AGT-LRx 80 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 43 | 319.86 nmol/L | Standard Deviation 180.741 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 169 | 700.48 nmol/L | Standard Deviation 195.702 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 15 | 446.29 nmol/L | Standard Deviation 189.521 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 29 | 293.27 nmol/L | Standard Deviation 129.051 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 43 | 239.02 nmol/L | Standard Deviation 133.633 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 57 | 293.12 nmol/L | Standard Deviation 157.651 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 85 | 321.71 nmol/L | Standard Deviation 176.356 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 92 | 317.93 nmol/L | Standard Deviation 159.204 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 106 | 443.95 nmol/L | Standard Deviation 196.226 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 120 | 562.27 nmol/L | Standard Deviation 202.035 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 148 | 662.13 nmol/L | Standard Deviation 130.207 |
| IONIS-AGT-LRx 120 mg | Absolute Concentration of Plasma AGT at Each Scheduled, Post-Baseline Visit | At Day 71 | 308.86 nmol/L | Standard Deviation 156.533 |
Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit
Time frame: Baseline, Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of the 12 doses of study drug, did not alter antihypertensive medications during the treatment period and prior to Day 85, and had no significant protocol deviations that would have been expected to affect efficacy assessment. 'Number analyzed' indicates the number of participants with data available for analysis at the specified time point.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 71 | -47.31 nmol/L | Standard Deviation 239.488 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Baseline | 833.42 nmol/L | Standard Deviation 196.561 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 15 | 44.94 nmol/L | Standard Deviation 137.033 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 29 | 3.31 nmol/L | Standard Deviation 132.768 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 43 | 8.15 nmol/L | Standard Deviation 152.008 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 57 | 15.03 nmol/L | Standard Deviation 182.246 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 85 | -39.65 nmol/L | Standard Deviation 171.289 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 92 | -73.33 nmol/L | Standard Deviation 153.744 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 106 | -57.84 nmol/L | Standard Deviation 169.818 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 120 | -64.61 nmol/L | Standard Deviation 131.455 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 148 | -62.29 nmol/L | Standard Deviation 153.117 |
| Pooled Placebo | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 169 | -18.31 nmol/L | Standard Deviation 170.377 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 169 | -189.48 nmol/L | Standard Deviation 260.868 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 71 | -578.49 nmol/L | Standard Deviation 276.95 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 85 | -544.60 nmol/L | Standard Deviation 314.195 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 106 | -449.05 nmol/L | Standard Deviation 288.731 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Baseline | 877.70 nmol/L | Standard Deviation 290.487 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 57 | -577.72 nmol/L | Standard Deviation 282.528 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 148 | -225.14 nmol/L | Standard Deviation 233.595 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 15 | -303.67 nmol/L | Standard Deviation 187.426 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 92 | -542.20 nmol/L | Standard Deviation 281.935 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 43 | -557.84 nmol/L | Standard Deviation 267.373 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 29 | -489.09 nmol/L | Standard Deviation 260.294 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 120 | -341.33 nmol/L | Standard Deviation 259.403 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 29 | -543.33 nmol/L | Standard Deviation 211.294 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 43 | -544.34 nmol/L | Standard Deviation 227.409 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 120 | -282.34 nmol/L | Standard Deviation 182.477 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 57 | -542.84 nmol/L | Standard Deviation 223.631 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 85 | -517.42 nmol/L | Standard Deviation 230.73 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 92 | -523.31 nmol/L | Standard Deviation 219.037 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 148 | -165.06 nmol/L | Standard Deviation 139.585 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 71 | -522.65 nmol/L | Standard Deviation 216.465 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Baseline | 836.60 nmol/L | Standard Deviation 189.204 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 106 | -395.60 nmol/L | Standard Deviation 218.864 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 15 | -390.31 nmol/L | Standard Deviation 189.039 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Plasma AGT to Each Scheduled, Post-Baseline Visit | Change From Baseline at Day 169 | -129.72 nmol/L | Standard Deviation 146.013 |
Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit
Time frame: Baseline, Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of 12 doses of study drug, did not alter antihypertensive medications during treatment period and prior to Day 85,and had no significant protocol deviations that would have been expected to affect efficacy assessment. 'Number analyzed' is the number of participants with data available for analysis at the specified timepoint
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -5.20 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -4.72 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -4.78 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -5.07 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -8.06 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -5.50 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -7.83 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -7.52 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -5.93 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -7.59 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -4.07 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -5.61 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -4.87 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -4.67 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -6.13 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -6.37 mmHg |
| Pooled Placebo | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -6.05 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -6.11 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -3.47 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -4.70 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -5.62 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -6.72 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -6.32 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -6.87 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -5.99 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -7.90 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -5.73 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -5.36 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -6.78 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -5.82 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -5.94 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -3.50 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -4.80 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -5.34 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -4.38 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -6.13 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -3.90 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -1.54 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -4.87 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -4.84 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -3.86 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -4.85 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -4.31 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -4.25 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -5.26 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -4.68 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -6.46 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -6.26 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -3.29 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -5.87 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office DBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -5.42 mmHg |
Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit
Time frame: Baseline, Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of 12 doses of study drug did not alter antihypertensive medications during treatment period \& prior to Day 85 have no significant protocol deviations that would be expected to affect efficacy assessment. 'Number analyzed' indicates number of participants with data available for analysis at specified time point.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -9.64 mmHg | Standard Deviation 16.346 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -10.93 mmHg | Standard Deviation 12.25 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -7.38 mmHg | Standard Deviation 14.967 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -14.19 mmHg | Standard Deviation 11.827 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -10.13 mmHg | Standard Deviation 13.844 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -9.31 mmHg | Standard Deviation 11.853 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -12.26 mmHg | Standard Deviation 14.671 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -13.31 mmHg | Standard Deviation 13.019 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -9.36 mmHg | Standard Deviation 13.24 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -9.50 mmHg | Standard Deviation 15.725 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -7.98 mmHg | Standard Deviation 13.973 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -12.14 mmHg | Standard Deviation 13.258 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -9.49 mmHg | Standard Deviation 16.385 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -9.23 mmHg | Standard Deviation 13.336 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -11.76 mmHg | Standard Deviation 18.127 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -11.48 mmHg | Standard Deviation 15.953 |
| Pooled Placebo | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -9.07 mmHg | Standard Deviation 13.65 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -9.37 mmHg | Standard Deviation 16.435 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -5.87 mmHg | Standard Deviation 12.427 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -7.73 mmHg | Standard Deviation 13.768 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -7.84 mmHg | Standard Deviation 16.1 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -9.13 mmHg | Standard Deviation 14.258 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -11.73 mmHg | Standard Deviation 15.193 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -9.64 mmHg | Standard Deviation 17.112 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -9.89 mmHg | Standard Deviation 14.257 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -7.70 mmHg | Standard Deviation 14.305 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -8.35 mmHg | Standard Deviation 15.426 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -11.57 mmHg | Standard Deviation 13.971 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -10.93 mmHg | Standard Deviation 15.319 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -7.57 mmHg | Standard Deviation 15.855 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -8.57 mmHg | Standard Deviation 16.476 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -5.14 mmHg | Standard Deviation 15.514 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -6.76 mmHg | Standard Deviation 15.637 |
| IONIS-AGT-LRx 80 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -8.76 mmHg | Standard Deviation 16.798 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 8 | -4.78 mmHg | Standard Deviation 13.306 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 85 | -6.98 mmHg | Standard Deviation 15.995 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 29 | -6.91 mmHg | Standard Deviation 12.096 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 169 | -2.02 mmHg | Standard Deviation 17.468 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 92 | -6.57 mmHg | Standard Deviation 13.11 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 22 | -6.80 mmHg | Standard Deviation 13.881 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 148 | -4.30 mmHg | Standard Deviation 14.393 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 106 | -6.61 mmHg | Standard Deviation 16.158 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 15 | -4.11 mmHg | Standard Deviation 11.443 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 64 | -8.19 mmHg | Standard Deviation 15.241 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 57 | -7.47 mmHg | Standard Deviation 18.194 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 36 | -6.40 mmHg | Standard Deviation 14.318 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 71 | -5.71 mmHg | Standard Deviation 16.045 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 50 | -6.13 mmHg | Standard Deviation 16.453 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 120 | -5.14 mmHg | Standard Deviation 15.02 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 78 | -8.22 mmHg | Standard Deviation 14.734 |
| IONIS-AGT-LRx 120 mg | Change From Baseline in Seated Automated Office SBP to Each Scheduled, Post-Baseline Visit | Change from Baseline at Day 43 | -7.24 mmHg | Standard Deviation 16.563 |
Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM)
Time frame: Baseline, Day 85
Population: PPS included all FAS participants who received at least 10 of the 12 doses of study drug, did not alter antihypertensive medications during the Treatment Period and prior to Study Day 85, and have no significant protocol deviations that would be expected to affect efficacy assessment. 'Overall number of participants analyzed' indicates the number of participants with data available for the analysis of this outcome measure.
| Arm | Measure | Group | Value (LEAST_SQUARES_MEAN) |
|---|---|---|---|
| Pooled Placebo | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean SBP at Day 85 | -1.362 mmHg |
| Pooled Placebo | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean DBP at Day 85 | -1.667 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean DBP at Day 85 | -4.406 mmHg |
| IONIS-AGT-LRx 80 mg | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean SBP at Day 85 | -5.675 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean DBP at Day 85 | -2.792 mmHg |
| IONIS-AGT-LRx 120 mg | Change From Baseline to Study Day 85 in 24-hour Mean SBP and Diastolic Blood Pressure (DBP) Measured by Ambulatory Blood Pressure Monitoring (ABPM) | Change from Baseline in 24-hour Mean SBP at Day 85 | -0.862 mmHg |
Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit
Time frame: Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169
Population: PPS analysis set was used. Participants with SBP ≤ 140 mmHg at baseline were excluded from this analysis. 'Overall number of participants analyzed' indicates the number of participants with data available for the analysis of this outcome measure. 'Number analyzed' indicates number of participants with data available for analysis at specified time point.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 8 | 37.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 120 | 51.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 169 | 86.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 169 | 50.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 106 | 86.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 148 | 82.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 8 | 81.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 85 | 40.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 120 | 81.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 15 | 78.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 29 | 46.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 92 | 82.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 22 | 87.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 169 | 50.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 85 | 81.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 29 | 81.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 78 | 56.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 78 | 93.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 36 | 83.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 36 | 48.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 71 | 93.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 43 | 90.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 120 | 51.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 64 | 96.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 50 | 87.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 71 | 48.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 57 | 90.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 43 | 40.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 29 | 46.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 64 | 59.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 50 | 58.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 148 | 44.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 8 | 37.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 57 | 46.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 64 | 59.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 57 | 46.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 50 | 58.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 71 | 48.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 106 | 55.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 43 | 40.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 78 | 56.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 15 | 31.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 36 | 45.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 85 | 40.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 148 | 37.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 22 | 28.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 92 | 55.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 92 | 51.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 15 | 28.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 106 | 55.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 22 | 31.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 78 | 46.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 120 | 48.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 148 | 48.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 22 | 65.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 29 | 50.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 8 | 38.5 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 15 | 53.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 22 | 65.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 29 | 53.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 36 | 60.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 43 | 69.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 50 | 57.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 57 | 53.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 64 | 36.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 71 | 48.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 78 | 50.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 85 | 64.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 92 | 52.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 106 | 60.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 169 | 58.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 8 | 73.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 15 | 80.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 22 | 88.5 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 29 | 88.5 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 36 | 92.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 43 | 84.6 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 50 | 96.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 57 | 80.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 64 | 80.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 71 | 84.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 78 | 84.6 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 85 | 88.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 92 | 88.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 106 | 95.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 120 | 72.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 148 | 80.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 169 | 83.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 8 | 34.6 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 15 | 50.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 36 | 57.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 43 | 65.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 50 | 57.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 57 | 50.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 64 | 36.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 71 | 44.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 85 | 60.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 92 | 48.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 106 | 60.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 120 | 44.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 148 | 44.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 169 | 54.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 148 | 95.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 148 | 34.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 15 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 169 | 87.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 106 | 56.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 169 | 37.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 8 | 36.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 92 | 23.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 92 | 23.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 15 | 36.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 85 | 33.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 29 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 78 | 58.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 8 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 36 | 52.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 71 | 56.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 148 | 34.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 43 | 41.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 64 | 68.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 106 | 52.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 50 | 37.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 57 | 56.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 22 | 36.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 57 | 52.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 43 | 45.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 120 | 43.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 64 | 63.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 50 | 83.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 36 | 52.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 57 | 82.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 43 | 79.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 120 | 39.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 64 | 86.4 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 36 | 92.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 71 | 52.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 71 | 92.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 29 | 80.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 29 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 78 | 79.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 22 | 72.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 50 | 41.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 85 | 83.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 15 | 88.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 78 | 54.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 22 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 106 | 82.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 8 | 72.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 92 | 85.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 90 mmHg at Day 120 | 95.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg at Day 169 | 37.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated Office SBP ≤ 140 mmHg, DBP ≤ 90 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 140 mmHg and DBP ≤ 90 mmHg at Day 85 | 33.3 percentage of participants |
Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit
Time frame: Days 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, 78, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of the 12 doses of study drug, did not alter antihypertensive medications during the Treatment Period and prior to study day 85, and have no significant protocol deviations that would be expected to affect efficacy assessment. 'Number analyzed' indicates the number of participants with data available for analysis at the specified time point.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 169 | 55.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 120 | 28.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 15 | 48.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 148 | 53.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 148 | 31.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 78 | 37.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 120 | 64.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 169 | 30.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 106 | 61.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 22 | 59.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 29 | 28.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 92 | 66.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 29 | 60.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 8 | 53.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 85 | 60.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 36 | 56.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 71 | 30.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 78 | 67.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 43 | 57.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 36 | 36.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 120 | 25.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 71 | 58.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 57 | 66.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 64 | 33.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 64 | 60.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 43 | 28.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 50 | 63.6 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 57 | 22.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 50 | 27.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 106 | 31.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 50 | 25.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 57 | 24.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 15 | 20.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 43 | 24.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 64 | 40.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 8 | 20.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 36 | 27.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 71 | 30.2 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 169 | 27.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 29 | 24.4 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 78 | 41.9 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 92 | 38.1 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 22 | 27.3 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 85 | 26.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 148 | 26.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 15 | 20.0 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 92 | 40.5 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 85 | 26.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 8 | 17.8 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 106 | 35.7 percentage of participants |
| Pooled Placebo | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 22 | 27.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 71 | 44.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 8 | 64.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 15 | 66.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 8 | 37.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 15 | 35.6 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 22 | 31.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 29 | 44.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 36 | 43.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 43 | 46.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 50 | 44.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 57 | 43.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 64 | 31.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 169 | 42.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 78 | 44.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 85 | 50.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 92 | 34.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 106 | 52.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 120 | 34.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 148 | 33.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 22 | 64.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 29 | 68.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 36 | 75.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 43 | 71.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 50 | 66.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 57 | 68.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 64 | 68.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 71 | 58.1 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 78 | 69.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 85 | 75.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 92 | 70.5 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 106 | 66.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 120 | 63.6 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 148 | 61.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 169 | 66.7 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 8 | 33.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 15 | 33.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 22 | 24.4 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 29 | 40.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 36 | 37.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 43 | 37.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 50 | 37.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 57 | 40.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 64 | 25.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 71 | 34.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 78 | 37.2 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 85 | 40.9 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 92 | 27.3 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 106 | 40.5 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 120 | 31.8 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 148 | 31.0 percentage of participants |
| IONIS-AGT-LRx 80 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 169 | 38.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 92 | 33.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 8 | 60.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 8 | 26.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 85 | 37.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 85 | 31.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 15 | 17.4 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 78 | 37.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 8 | 30.4 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 22 | 30.4 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 71 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 169 | 27.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 29 | 34.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 64 | 34.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 92 | 28.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 36 | 35.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 57 | 39.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 106 | 59.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 43 | 35.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 50 | 40.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 148 | 23.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 50 | 28.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 43 | 44.4 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 106 | 29.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 57 | 30.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 36 | 48.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 57 | 65.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 43 | 60.0 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 64 | 62.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 50 | 53.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 64 | 25.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 71 | 62.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 36 | 55.6 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 29 | 43.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 78 | 66.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 29 | 65.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 169 | 34.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 85 | 66.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 22 | 58.7 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 71 | 31.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 92 | 64.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 15 | 56.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 22 | 34.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 148 | 27.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 120 | 23.3 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 120 | 60.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 120 | 30.2 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg and DBP ≤ 80 mmHg at Day 78 | 37.8 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 148 | 60.5 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 106 | 40.9 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With SBP ≤ 130 mmHg at Day 15 | 26.1 percentage of participants |
| IONIS-AGT-LRx 120 mg | Percentage of Participants Who Achieved Seated Automated SBP ≤ 130 mmHg, DBP ≤ 80 mmHg, and Both at Each Scheduled Post-Baseline Visit | Percentage of Participants With DBP ≤ 80 mmHg at Day 169 | 48.8 percentage of participants |
Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit
Time frame: Baseline, Days 15, 29, 43, 57, 71, 85, 92, 106, 120, 148, and 169
Population: PPS included all FAS participants who received at least 10 of 12 doses of study drug did not alter antihypertensive medications during treatment period \& prior to Day 85 have no significant protocol deviations that would be expected to affect efficacy assessment. 'Number analyzed' indicates number of participants with data available for analysis at specified time point.
| Arm | Measure | Group | Value (MEAN) | Dispersion |
|---|---|---|---|---|
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 106 | -6.3 percent change | Standard Deviation 20.4 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 57 | 1.6 percent change | Standard Deviation 21.1 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 169 | -2.0 percent change | Standard Deviation 19.8 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 92 | -8.3 percent change | Standard Deviation 19.5 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 85 | -3.3 percent change | Standard Deviation 19.6 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 148 | -6.1 percent change | Standard Deviation 20 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 29 | 0.5 percent change | Standard Deviation 16.7 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 71 | -4.8 percent change | Standard Deviation 25.5 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 120 | -7.3 percent change | Standard Deviation 14.9 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 43 | 0.3 percent change | Standard Deviation 18.6 |
| Pooled Placebo | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 15 | 5.6 percent change | Standard Deviation 16.8 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 57 | -63.7 percent change | Standard Deviation 17.9 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 15 | -34.3 percent change | Standard Deviation 17.2 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 29 | -54.4 percent change | Standard Deviation 18.3 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 43 | -62.4 percent change | Standard Deviation 16.5 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 71 | -63.3 percent change | Standard Deviation 19.4 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 85 | -59.2 percent change | Standard Deviation 27.4 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 92 | -60.0 percent change | Standard Deviation 18.7 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 106 | -47.6 percent change | Standard Deviation 22.8 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 120 | -36.3 percent change | Standard Deviation 20.6 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 148 | -22.8 percent change | Standard Deviation 25.4 |
| IONIS-AGT-LRx 80 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 169 | -18.3 percent change | Standard Deviation 29.6 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 148 | -18.4 percent change | Standard Deviation 15.9 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 106 | -46.4 percent change | Standard Deviation 21.9 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 29 | -63.6 percent change | Standard Deviation 17.5 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 57 | -64.0 percent change | Standard Deviation 18.3 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 120 | -33.2 percent change | Standard Deviation 20 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 15 | -46.4 percent change | Standard Deviation 18.8 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 85 | -60.7 percent change | Standard Deviation 23.1 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 71 | -62.0 percent change | Standard Deviation 19 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 169 | -15.2 percent change | Standard Deviation 17.3 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 92 | -61.4 percent change | Standard Deviation 19 |
| IONIS-AGT-LRx 120 mg | Percent Change From Baseline in Plasma AGT at Each Scheduled, Post-Baseline Visit | Percent Change from Baseline at Day 43 | -63.2 percent change | Standard Deviation 20.4 |