Efficacy and safety of a single-pill versus free combination of perindopril/indapamide/amlodipine: a multicenter, randomized, double-blind study in Chinese patients with hypertension

Author:

Wang Ji-Guang1,Topouchian Jirar2,Bricout-Hennel Stéphanie3,Mu Jianjun4,Chen Lianglong5,Li Ping6,He Shenghu7,Luo Suxin8,Jiang Weihong9,Jiang Yinong10,Sun Yuemin11,Zhang Yuqing12,Asmar Roland13

Affiliation:

1. Department of Hypertension, The Shanghai Institute of Hypertension, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China

2. Paris Descartes University, AP-HP, Diagnosis and Therapeutic Center, Hôtel-Dieu

3. Institut de Recherches Internationales Servier, Paris-Saclay, France

4. Department of Cardiology, First Affiliated Hospital, School of Medicine of Xi’an Jiaotong University, Xi’an, Shaanxi

5. Department of Cardiology, Fujian Medical University Union Hospital, Fuzhou, Fujian

6. Department of Cardiology, Second affiliated hospital of Nanchang University, Nanchang, Jiangxi

7. Department of Cardiology, Northern Jiangsu People's Hospital, Yangzhou, Jiangsu

8. Department of Cardiology, First affiliated hospital, Chongqing Medical University Chongqing

9. Department of Cardiology, Third Xiangya Hospital of Central South University, Changsha, Hunan

10. Department of Cardiology, First affiliated hospital of Dalian Medical University, Dalian, Liaoning

11. Department of Cardiology, Tianjin Medical University General Hospital, Tianjin

12. Department of Cardiology, Affiliated Jiangning Hospital of Nanjing Medical University, Nanjing, Jiangsu, China

13. Foundation-Medical Research Institutes, Geneva, Switzerland

Abstract

Background: In China, the prevalence of hypertension is high and the use of combination antihypertensive therapy is low, which contributes to inadequate blood pressure (BP) control. The availability of simplified treatments combining complementary BP-lowering agents may help more patients achieve their goals. Methods: This Phase III, multicenter, randomized, double-blind, noninferiority study included Chinese adults with mild-to-moderate hypertension. Following a 1-month run-in on perindopril/indapamide bi-therapy, patients with uncontrolled systolic/diastolic BP (≥140/90 mmHg) were randomized to perindopril 5 mg/indapamide 1.25 mg/amlodipine 5 mg (Per/Ind/Aml) single-pill combination (SPC) or perindopril 4 mg/indapamide 1.25 mg plus amlodipine 5 mg (Per/Ind + Aml) for 6 months. Uptitration was permitted from month 2 onwards. The primary efficacy objective was the noninferiority of Per/Ind/Aml in lowering office systolic BP at 2 months. The secondary objectives included the effectiveness of SPC on diastolic BP, uptitration efficacy, and office BP control (systolic/diastolic <140/90 mmHg). A subgroup of patients participated in 24-h ambulatory BP monitoring (ABPM). Results: A total of 532 patients were randomized: Per/Ind/Aml (n = 262) and Per/Ind + Aml (n = 269). Overall, the mean (±SD) age was 55.7 ± 8.8 years, 60.7% were male, and the mean office systolic/diastolic BP at baseline on Per/Ind was 150.4/97.2 mmHg. Systolic BP decreased in both groups at 2 months from baseline: −14.99 ± 14.46 mmHg Per/Ind/Aml versus −14.49 ± 12.87 mmHg Per/Ind +Aml. A predefined noninferiority margin of 4 mmHg was observed (P < 0.001). The effectiveness of the Per/Ind/Aml SPC was also demonstrated for all secondary endpoints. ABPM demonstrated sustained BP control over 24 h. Both treatments were well tolerated. Conclusions: Per/Ind/Aml is an effective substitute for Per/Ind + Aml, providing at least equivalent BP control over 24 h in a single pill, with comparable safety.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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