摘要

Background:Azilsartan medoxomil (AZL-M), an angiotensin II receptor blocker, has been developed in fixed-dose combinations (FDCs) with chlorthalidone (CTD).Objective/methods:We compared FDCs of AZL-M/CTD 20/12.5mg once daily titrated to 40/25mg if needed or AZL-M/CTD 40/12.5mg once daily titrated to 80/25mg if needed with an olmesartan medoxomil (OLM)-hydrochlorothiazide (HCTZ) 20/12.5mg FDC once daily titrated to 40/25mg if needed in a randomized, double-blind, 8-week study of 1085 participants with clinic SBP 160-190mmHg and DBP 119mmHg or less. Titration to higher doses occurred at week 4 if BP was at least 140/90mmHg (130/80mmHg if diabetes or chronic kidney disease). The primary endpoint was change from baseline in clinic SBP; 24-h ambulatory BP monitoring was also measured.Results:Greater reductions in clinic SBP from a baseline of 165mmHg were observed (P<0.001) in both AZL-M/CTD arms (-37.6 and -38.2mmHg) versus OLM/HCTZ (-31.5mmHg), despite greater dose titration in the OLM/HCTZ group. At 8 weeks, both AZL-M/CTD FDCs reduced 24-h SBP more than OLM/HCTZ (-26.4 and -27.9 versus -20.7mmHg; both P<0.001), and higher proportions in both AZL-M/CTD groups achieved target BP compared with the OLM/HCTZ group (69.4 and 68.9 versus 54.7%, both P<0.001). Adverse events leading to drug discontinuation occurred in 6.2, 9.5, and 3.1% with the AZL-M/CTD lower and higher doses, and OLM/HCTZ, respectively.Conclusion:This large, titration-to-target BP study demonstrated AZL-M/CTD FDCs to have superior antihypertensive efficacy compared with the maximum approved dose of OLM/HCTZ.

  • 出版日期2018-4