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Evaluation of the angiotensin II receptor blocker azilsartan medoxomil in African-American patients with hypertension.
Johnson, Wallace; White, William B; Sica, Domenic; Bakris, George L; Weber, Michael A; Handley, Alison; Perez, Alfonso; Cao, Charlie; Kupfer, Stuart; Saunders, Elijah B.
Afiliación
  • Johnson W; University of Maryland School of Medicine, Baltimore, MD, USA.
  • White WB; Cardiology Center, University of Connecticut School of Medicine, Farmington, CT, USA.
  • Sica D; Virginia Commonwealth University Health System, Richmond, VA, USA.
  • Bakris GL; University of Chicago Medicine, Chicago, IL, USA.
  • Weber MA; SUNY Downstate College of Medicine, New York, NY, USA.
  • Handley A; Takeda Pharmaceuticals International Inc., Deerfield, IL, USA.
  • Perez A; Takeda Development Center Americas Inc., Deerfield, IL, USA.
  • Cao C; Takeda Pharmaceuticals America, Inc.
  • Kupfer S; Takeda Development Center Americas Inc., Deerfield, IL, USA.
  • Saunders EB; University of Maryland School of Medicine, Baltimore, MD, USA.
J Clin Hypertens (Greenwich) ; 19(7): 695-701, 2017 Jul.
Article en En | MEDLINE | ID: mdl-28493376
The efficacy and safety of azilsartan medoxomil (AZL-M) were evaluated in African-American patients with hypertension in a 6-week, double-blind, randomized, placebo-controlled trial, for which the primary end point was change from baseline in 24-hour mean systolic blood pressure (BP). There were 413 patients, with a mean age of 52 years, 57% women, and baseline 24-hour BP of 146/91 mm Hg. Treatment differences in 24-hour systolic BP between AZL-M 40 mg and placebo (-5.0 mm Hg; 95% confidence interval, -8.0 to -2.0) and AZL-M 80 mg and placebo (-7.8 mm Hg; 95% confidence interval, -10.7 to -4.9) were significant (P≤.001 vs placebo for both comparisons). Changes in the clinic BPs were similar to the ambulatory BP results. Incidence rates of adverse events were comparable among the treatment groups, including those of a serious nature. In African-American patients with hypertension, AZL-M significantly reduced ambulatory and clinic BPs in a dose-dependent manner and was well tolerated.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Sanguínea / Monitoreo Ambulatorio de la Presión Arterial / Antagonistas de Receptores de Angiotensina / Hipertensión Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: J Clin Hypertens (Greenwich) Asunto de la revista: ANGIOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Presión Sanguínea / Monitoreo Ambulatorio de la Presión Arterial / Antagonistas de Receptores de Angiotensina / Hipertensión Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: J Clin Hypertens (Greenwich) Asunto de la revista: ANGIOLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos