
Baxdrostat, a new hypertension medication undergoing Phase 2 trials, was not associated with a reduction in blood pressure when compared to placebo in patients with resistant hypertension, according to results from the newly released HALO trial.
The role of hypertension and adverse health outcomes has been well established in the medical literature. Concerningly, an estimated 10 million Americans suffer from “treatment resistant hypertension,” or uncontrolled blood pressure despite at least three blood-pressure lowering medications (Carey et al). The need for pharmacotherapy in this population is critical, explained a speaker at 2023 American College of Cardiology (ACC) Scientific Session.
Dr. Deepak Bhatt, MD, MPH, the Director of Mount Sinai Heart, described the results of the HALO trial, a phase 2 randomized controlled trial evaluating the efficacy of baxdrostat at the ACC Scientific Session in New Orleans, LA. Resistant hypertension has been strongly linked to the renin-angiotensin-aldosterone system, with observational data demonstrating the role of aldosterone excess in contributing to high blood pressure. Prior randomized controlled trials (PATHWAY-2) and metanalyses showed that mineralocorticoid receptor antagonists (MRAs), which block the effect of aldosterone, were among the most effective medications at reducing blood pressure (Yugar Toledo et al). This led to significant excitement when baxdrostat, a selective aldosterone synthase inhibitor, was shown to cause a sustained, dose-dependent reduction in plasma aldosterone levels in a Phase 1 trial. Additionally, baxdrostat reduced systolic blood pressure in patients with resistant hypertension by 11 mm Hg when compared to placebo in a separate Phase 2 study, BrigHTN (Freeman et al).