on behalf of the trial investigators 9This 8-week, randomized, double-blind, parallel-group study compared the efficacy and safety of aliskiren with ramipril in Asian patients with mild to moderate hypertension. Following a 2-to 3-week placebo run-in period, patients with mean sitting diastolic blood pressure (msDBP) X95 and o110 mm Hg were randomized to receive once daily dose of either aliskiren 75, 150, 300 mg or ramipril 5 mg for 8 weeks. Efficacy variables were the changes in msDBP and mean sitting systolic BP (msSBP) and BP control rates (o140/90 mm Hg). Safety was assessed by recording adverse events (AEs) and serious AEs (SAEs). Of 1316 randomized patients, 1160 (88.1%) completed the study. At the study endpoint, patients on aliskiren had greater mean BP reductions (14.39/11.63 mm Hg for 300 mg; 12.16/10.04 mm Hg for 150 mg; 12.24/10.66 mm Hg for 75 mg) than those on 5 mg ramipril (11.46/9.19 mm Hg). All aliskiren doses were statistically non-inferior (Po0.0001) to ramipril in reducing msDBP. The reduction in BP for aliskiren 300 mg was statistically superior vs. ramipril (Po0.002). Blood pressure control rates were higher for aliskiren (300 mg, 52.29%; 150 mg, 48.11%; 75 mg, 45.68%) than for ramipril (5 mg, 43.7%); the difference for aliskiren 300 mg vs. ramipril 5 mg was statistically significant (Po0.05). Aliskiren was well tolerated with a fourfold lower incidence of cough (0.6-1.2%) compared with ramipril (5.2%). SAEs were rare in this study (0.5%). Aliskiren produced greater BP reductions with a lower incidence of cough than ramipril in Asian patients with mild to moderate hypertension. Hypertension Research (2012) 35, 28-33; doi:10.1038/hr.2011.150; published online 8 September 2011Keywords: aliskiren; Asian; cough; ramipril INTRODUCTION Despite advances in the diagnosis and treatment of hypertension, only about 5-33% of patients achieve blood pressure (BP) control (o140/ 90 mm Hg) globally. Blood pressure control rates for the Asian population range from 9.5 to 36.6%, and in China, the rates have been estimated to be as low as 9.5%. This is of particular concern because of the increasing prevalence of hypertension (15-35%) in the Asian populations. [1][2][3][4][5][6][7] Of the many available antihypertensive drugs, angiotensin-converting enzyme inhibitors (ACEis) and angiotensin II receptor blockers that act on the renin angiotensin-aldosterone system form the mainstay of therapy today. 2,8 However, incomplete blockade of renin angiotensin-aldosterone system by these agents results in an increase in plasma renin activity and potentially limits the therapeutic benefits of these drugs. 9 Moreover, ACE inhibition also results in suppression of kininase II, which may be followed by accumulation of the protussive mediators bradykinin and substance P in the upper respiratory tract or lungs. This results in undesirable adverse effects,