drugset / Trial / NCT06344104

A Study to Investigate the Efficacy and Safety of Baxdrostat in Participants With Uncontrolled Hypertension on Two or More Medications Including Participants With Resistant Hypertension

NCT06344104

Phase 3 Completed 326 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to measure the efficacy and safety of baxdrostat in participants with uHTN or rHTN. The main objective is to compare the difference in SBP change from baseline at Week 12 of treatment between participants receiving 2 mg baxdrostat or 1 mg baxdrostat tablets and participants receiving placebo tablets.

Timeline

Start
2024-04-08
Primary completion
2025-11-24
Completion
2026-04-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Baxdrostat Small molecule 1 mg Oral
Subject Baxdrostat Small molecule 2 mg Oral