Promising Results for Lorundrostat in Treating Resistant Hypertension
Recent studies have shown that Lorundrostat, a new medication targeting aldosterone synthesis, demonstrates significant potential in managing resistant hypertension. This condition, characterized by high blood pressure that remains uncontrolled despite the use of multiple antihypertensive drugs, poses a considerable challenge for both patients and healthcare providers.
Aldosterone, a mineralocorticoid produced in the adrenal glands, plays a crucial role in regulating blood pressure, fluid balance, and electrolytes in the body. It promotes sodium retention and potassium excretion in the kidneys, leading to increased blood volume and pressure. For patients suffering from secondary hyperaldosteronism, often seen in cases of heart failure, traditional treatment options like aldosterone antagonists (e.g., spironolactone) may not be suitable due to compensatory increases in serum aldosterone levels and various off-target effects that can lead to poor patient adherence.
The recent article published in the New England Journal of Medicine highlights how dysregulation of aldosterone is frequently observed in patients with uncontrolled hypertension. Given the limitations of existing treatments, there is a growing interest in aldosterone synthase inhibitors (ASIs) such as Lorundrostat, which selectively target the aldosterone synthesis pathway without affecting cortisol production.
In a Phase IIb clinical trial known as Advance-HTN, conducted at 103 centers across the United States, researchers assessed the efficacy of Lorundrostat in adults whose blood pressure remained elevated despite taking two to five antihypertensive medications. Participants initially ceased their existing blood pressure medications and were switched to a standardized regimen consisting of an AT1 antagonist (Olmesartan) and a diuretic (Indapamide or Hydrochlorothiazide). Those previously on a more extensive medication regimen also received the calcium channel blocker Amlodipine.
After three weeks on the standardized treatment, 285 participants whose 24-hour blood pressure measurements remained above 130/80 mmHg entered the trial's main phase. Among them, 94 received a fixed dose of 50 mg of Lorundrostat daily, while 96 began with 50 mg daily and could increase to 100 mg depending on their systolic blood pressure response. The remaining 95 participants were given a placebo.
The results from this trial are significant, indicating that Lorundrostat may provide a new therapeutic avenue for patients struggling with resistant hypertension. As current treatment options remain inadequate for many, the implications of this research could lead to improved management strategies for affected individuals.