Azilsartan Medoxomil Plus Chlorthalidone Reduces Blood Pressure More Effectively Than Olmesartan Plus Hydrochlorothiazide in Stage 2 Systolic Hypertension

Author:

Cushman William C.1,Bakris George L.1,White William B.1,Weber Michael A.1,Sica Domenic1,Roberts Andrew1,Lloyd Eric1,Kupfer Stuart1

Affiliation:

1. From the University of Tennessee College of Medicine (W.C.C.), Memphis, TN; The University of Chicago Medicine (G.L.B.), Chicago, IL; University of Connecticut School of Medicine (W.B.W.), Farmington, CT; Downstate Medical Center (M.A.W.), Brooklyn, NY; Virginia Commonwealth University (D.S.), Richmond, VA; Takeda Global Research and Development Center, Inc (A.R., E.L., S.K.), Deerfield, IL.

Abstract

Azilsartan medoxomil, an effective, long-acting angiotensin II receptor blocker, is a new treatment for hypertension that is also being developed in fixed-dose combinations with chlorthalidone, a potent, long-acting thiazide-like diuretic. We compared once-daily fixed-dose combinations of azilsartan medoxomil/chlorthalidone force titrated to a high dose of either 40/25 mg or 80/25 mg with a fixed-dose combination of the angiotensin II receptor blocker olmesartan medoxomil plus the thiazide diuretic hydrochlorothiazide force titrated to 40/25 mg. The design was a randomized, 3-arm, double-blind, 12-week study of 1071 participants with baseline clinic systolic blood pressure 160 to 190 mm Hg and diastolic blood pressure ≤119 mm Hg. Patients had a mean age of 57 years; 59% were men, 73% were white, and 22% were black. At baseline, mean clinic blood pressure was 165/96 mm Hg and 24-hour mean blood pressure was 150/88 mm Hg. Changes in clinic (primary end point) and ambulatory systolic blood pressures at week 12 were significantly greater in both azilsartan medoxomil/chlorthalidone arms than in the olmesartan/hydrochlorothiazide arm ( P <0.001). Changes in clinic systolic blood pressure (mean±SE) were −42.5±0.8, −44.0±0.8, and −37.1±0.8 mm Hg, respectively. Changes in 24-hour ambulatory systolic blood pressure were −33.9±0.8, −36.3±0.8, and −27.5±0.8 mm Hg, respectively. Adverse events leading to permanent drug discontinuation occurred in 7.9%, 14.5%, and 7.1% of the groups given azilsartan medoxomil/chlorthalidone 40/25 mg, azilsartan medoxomil/chlorthalidone 80/25 mg, and olmesartan/hydrochlorothiazide 40/25 mg, respectively. This large, forced-titration study has demonstrated superior antihypertensive efficacy of azilsartan medoxomil/chlorthalidone fixed-dose combinations compared with the maximum approved dose of olmesartan/hydrochlorothiazide.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

Reference30 articles.

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