Phase 2 Trial of Baxdrostat for Treatment-Resistant Hypertension

被引:225
作者
Freeman, Mason W. W. [1 ]
Halvorsen, Yuan-Di [1 ]
Marshall, William [1 ]
Pater, Mackenzie [3 ]
Isaacsohn, Jon [3 ]
Pearce, Catherine [1 ]
Murphy, Brian
Alp, Nicholas [4 ]
Srivastava, Ajay [4 ]
Bhatt, Deepak L. L. [2 ]
Brown, Morris J. J. [5 ]
机构
[1] CinCor Pharm, Boston, MA USA
[2] Harvard Med Sch, Brigham & Womens Hosp, Boston, MA USA
[3] CinRx Pharma, Cincinnati, OH USA
[4] Medpace, Cincinnati, OH USA
[5] Queen Mary Univ London, William Harvey Res Inst, Dept Clin Pharmacol, London, England
基金
英国医学研究理事会;
关键词
BLOOD-PRESSURE; DOUBLE-BLIND; ALDOSTERONE; HYPERKALEMIA; INHIBITION; THERAPY;
D O I
10.1056/NEJMoa2213169
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Aldosterone synthase controls the synthesis of aldosterone and has been a pharmacologic target for the treatment of hypertension for several decades. Selective inhibition of aldosterone synthase is essential but difficult to achieve because cortisol synthesis is catalyzed by another enzyme that shares 93% sequence similarity with aldosterone synthase. In preclinical and phase 1 studies, baxdrostat had 100:1 selectivity for enzyme inhibition, and baxdrostat at several dose levels reduced plasma aldosterone levels but not cortisol levels. Methods In this multicenter, placebo-controlled trial, we randomly assigned patients who had treatment-resistant hypertension, with blood pressure of 130/80 mm Hg or higher, and who were receiving stable doses of at least three antihypertensive agents, including a diuretic, to receive baxdrostat (0.5 mg, 1 mg, or 2 mg) once daily for 12 weeks or placebo. The primary end point was the change in systolic blood pressure from baseline to week 12 in each baxdrostat group as compared with the placebo group. Results A total of 248 patients completed the trial. Dose-dependent changes in systolic blood pressure of -20.3 mm Hg, -17.5 mm Hg, -12.1 mm Hg, and -9.4 mm Hg were observed in the 2-mg, 1-mg, 0.5-mg, and placebo groups, respectively. The difference in the change in systolic blood pressure between the 2-mg group and the placebo group was -11.0 mm Hg (95% confidence interval [CI], -16.4 to -5.5; P < 0.001), and the difference in this change between the 1-mg group and the placebo group was -8.1 mm Hg (95% CI, -13.5 to -2.8; P=0.003). No deaths occurred during the trial, no serious adverse events were attributed by the investigators to baxdrostat, and there were no instances of adrenocortical insufficiency. Baxdrostat-related increases in the potassium level of 6.0 mmol per liter or greater occurred in 2 patients, but these increases did not recur after withdrawal and reinitiation of the drug. Conclusions Patients with treatment-resistant hypertension who received baxdrostat had dose-related reductions in blood pressure.
引用
收藏
页码:395 / 405
页数:11
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