A Phase 3b, Double-Blind, Randomized, 12-Week Efficacy and Safety Study Comparing the TAK-491 Plus Chlorthalidone Fixed-Dose Combination vs Olmesartan Medoxomil-Hydrochlorothiazide in Subjects With Moderate to Severe Hypertension
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 1,071
- 主要终点
- Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.
研究概览
简要总结
The purpose of this study is to compare the antihypertensive effect of azilsartan medoxomil plus chlorthalidone, once daily (QD), to olmesartan medoxomil plus hydrochlorothiazide in participants with moderate to severe hypertension.
详细描述
According to the World Health Organization, hypertension is the most common attributable cause of preventable death in developed nations, as uncontrolled hypertension greatly increases the risk of cardiovascular disease, cerebrovascular disease, and renal failure. As the population ages, the prevalence of hypertension will continue to increase if broad and effective preventive measures are not implemented. Despite the availability of antihypertensive agents, hypertension remains inadequately controlled; only about one third of patients continue to maintain control successfully.
Treatment algorithms for essential hypertension commonly include thiazides or thiazide-like diuretics, either alone or as part of combination treatment. Chlorthalidone is a commercially available, orally administered thiazide-type diuretic agent.
TAK-491 (azilsartan medoxomil) is an angiotensin II receptor blocker developed by Takeda to treat participants with essential hypertension.
This study will compare the safety and tolerability of azilsartan medoxomil plus chlorthalidone (TAK-491CLD) fixed-dose combination to olmesartan medoxomil plus hydrochlorothiazide fixed-dose combination.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Has a mean sitting clinic systolic blood pressure greater than or equal to 160 and less than or equal to 190 mm Hg.
- •Females of childbearing potential who are sexually active agree to routinely use adequate contraception from Screening through 30 days after the last administered study drug dose.
- •Has clinical laboratory test results within the reference range for the testing laboratory or the investigator does not consider the results to be clinically significant.
- •Is willing to discontinue current antihypertensive medications on Day -21 or Day -28 if the participant is on amlodipine or chlorthalidone.
排除标准
- •Has a mean sitting clinic diastolic blood pressure greater than 119 mm Hg on Day -
- •Has a baseline 24-hour ambulatory blood pressure monitoring reading of insufficient quality.
- •Works a night (third) shift.
- •Has an upper arm circumference less than 24 cm or greater than 42 cm.
- •Has secondary hypertension of any etiology.
- •Has a recent history of myocardial infarction, heart failure, unstable angina, coronary artery bypass graft, percutaneous coronary intervention, hypertensive encephalopathy, cerebrovascular accident, or transient ischemic attack.
- •Has clinically significant cardiac conduction defects.
- •Has hemodynamically significant left ventricular outflow obstruction due to aortic valvular disease.
- •Has severe renal dysfunction or disease.
- •Has known or suspected unilateral or bilateral renal artery stenosis.
- •Has a history of cancer that has not been in remission for at least 5 years prior to the first dose of study drug.
- •Has poorly-controlled diabetes mellitus at Screening.
- •Has hypokalemia or hyperkalemia.
- •Has an alanine aminotransferase or aspartate aminotransferase level of greater than 2.5 times the upper limit of normal, active liver disease, or jaundice.
- •Has any other known serious disease or condition that would compromise safety, might affect life expectancy, or make it difficult to successfully manage and follow the participant according to the protocol.
- •Has known hypersensitivity to angiotensin II receptor blockers or thiazide-type diuretics or other sulfonamide-derived compounds.
- •Has a history of drug abuse or a history of alcohol abuse within the past 2 years.
研究组 & 干预措施
Azilsartan Medoxomil 20-40mg/Chlorthalidone 12.5-25mg QD
干预措施: Azilsartan medoxomil and chlorthalidone (Drug)
Azilsartan Medoxomil 40-80mg/Chlorthalidone 12.5-25mg QD
干预措施: Azilsartan medoxomil and chlorthalidone (Drug)
Olmesartan Medoxomil 20-40mg/Hydrochlorothiazide 12.5-25mg QD
干预措施: Olmesartan medoxomil and hydrochlorothiazide (Drug)
结局指标
主要结局
Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.
时间窗: Baseline and Week 12.
The change in sitting trough clinic systolic blood pressure measured at week 12 or final visit relative to baseline. Trough blood pressure is the average of the non-missing values of the 3 serial trough sitting systolic blood pressure measurements.
次要结局
- Change From Baseline in Trough, Sitting, Clinic Systolic Blood Pressure.(Baseline, Week 4 and Week 8.)
- Change From Baseline in Trough, Sitting, Clinic Diastolic Blood Pressure.(Baseline, Week 4, Week 8 and Week 12.)
- Change From Baseline in Mean Trough Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in 24-hour Mean Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in Mean Daytime (6 AM to 10 PM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in Mean Nighttime (12 AM to 6 AM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in the Mean Systolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in the Mean Diastolic Blood Pressure at 0 to 12 Hours After Dosing by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in the Mean Systolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in the Mean Diastolic Blood Pressure During Each Hour of the 24-hour Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Percentage of Participants Who Reached Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.(Baseline, Week 4, Week 8 and Week 12.)
- Change From Baseline in Mean Trough Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in 24-hour Mean Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in Mean Daytime (6 AM to 10 PM) Diastolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Change From Baseline in Mean Nighttime (12 AM to 6 AM) Systolic Blood Pressure by Ambulatory Blood Pressure Monitoring.(Baseline and Week 12.)
- Percentage of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline.(Baseline, Week 4, Week 8 and Week 12.)
- Percent of Participants Who Reached Target Clinic Systolic Blood Pressure of <140 mm Hg and/or Reduction of ≥20 mm Hg From Baseline and Target Clinic Diastolic Blood Pressure of <90 mm Hg and/or Reduction of ≥10 mm Hg From Baseline.(Baseline, Week 4, Week 8 and Week 12.)