AstraZeneca's Baxdrostat Shows Promise in Phase 3 Hypertension Trial

AstraZeneca's aldosterone synthase inhibitor baxdrostat has demonstrated significant efficacy in reducing blood pressure among patients with treatment-resistant hypertension, according to data presented at the American Heart Association 2025 Scientific Sessions. The phase 3 Bax24 trial results mark a crucial milestone for the pharmaceutical giant's $1.3 billion investment in CinCor Pharma, the original developer of baxdrostat.
Impressive Blood Pressure Reductions
The Bax24 trial, which enrolled 218 patients with treatment-resistant hypertension, showed that baxdrostat reduced ambulatory 24-hour average systolic blood pressure (SBP) by 14 mmHg compared to placebo over a 12-week period. This placebo-adjusted reduction is notably higher than the 7.9 mmHg drop reported for Mineralys Therapeutics' rival drug lorundrostat in similar trials.
Secondary endpoints also yielded positive results, with baxdrostat demonstrating statistically significant and clinically meaningful reductions in ambulatory nighttime average SBP (13.9 mmHg) and seated SBP (10.3 mmHg).
Competitive Advantage and Market Potential
Baxdrostat's extended half-life of 26 to 30 hours, compared to lorundrostat's 10 to 12 hours, is believed to be a key factor in its superior performance. This characteristic could provide AstraZeneca with a significant competitive edge in the hypertension market.
Sharon Barr, Executive Vice President of Biopharmaceuticals R&D at AstraZeneca, emphasized the drug's potential impact: "The Bax24 data demonstrate the significant impact that baxdrostat's long half-life and highly selective inhibition of aldosterone synthase can have in improving 24-hour and overnight blood pressure for patients with resistant hypertension."
Regulatory Path and Future Outlook
AstraZeneca has confirmed its intention to share the Bax24 trial data with regulatory authorities worldwide, although no specific timeline for approval submissions has been disclosed. The success of baxdrostat is crucial to AstraZeneca's ambitious plans to grow sales to $80 billion by 2030.
As the pharmaceutical landscape evolves, baxdrostat is poised to face competition from Mineralys Therapeutics' lorundrostat, which is also progressing through late-stage clinical development. The race to market between these two aldosterone synthase inhibitors could reshape the treatment paradigm for resistant hypertension in the coming years.
References
- AstraZeneca's $1.3B bet reduces blood pressure by 14 mmHg over 12 weeks in phase 3 win
AstraZeneca's aldosterone synthase inhibitor baxdrostat reduced blood pressure by 14 mmHg over 12 weeks, the pharma has said in a first look at the data from a key phase 3 win.
Explore Further
What are the safety profiles and potential side effects observed during the Bax24 trial for baxdrostat?
What is the competitive landscape for aldosterone synthase inhibitors in the resistant hypertension market?
How does baxdrostat's extended half-life specifically contribute to its efficacy over competing drugs like lorundrostat?
What is the estimated market size for resistant hypertension treatments globally and what portion could baxdrostat potentially capture?
What regulatory challenges or hurdles might AstraZeneca face in seeking approval for baxdrostat across different regions?