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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT06034743

Public ClinicalTrials.gov record NCT06034743. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 4:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy and Safety of Baxdrostat in Participants With Uncontrolled Hypertension on Two or More Medications Including Participants With Resistant Hypertension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase III, multicentre, randomised, double-blinded, placebo-controlled, parallel group study to evaluate the safety, tolerability and effect of 1 or 2 mg baxdrostat versus placebo, administered once daily (QD) orally, on the reduction of systolic blood pressure in approximately 720 participants aged ≥ 18 years with hypertension, despite a stable regimen of 2 antihypertensive agents at baseline, one of which is a diuretic (uncontrolled hypertension); or ≥ 3 antihypertensive agents at baseline, one of which is a diuretic (treatment-resistant hypertension).

Study identification

NCT ID
NCT06034743
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
796 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 22, 2023 (Actual)
Primary completion
May 21, 2025 (Actual)
Completion
Oct 10, 2025 (Actual)
Last update posted
Jul 30, 2026

2023 – 2025

United States locations

U.S. sites
43
U.S. states
24
U.S. cities
41
Facility City State ZIP Site status
Research Site Saraland Alabama 36571 —
Research Site Scottsdale Arizona 85054 —
Research Site Sun City West Arizona 85375 —
Research Site Surprise Arizona 85374 —
Research Site Little Rock Arkansas 72211 —
Research Site Fresno California 93720 —
Research Site Lincoln California 95648 —
Research Site Orange California 92868 —
Research Site Rancho Cucamonga California 91730 —
Research Site Stanford California 94304 —
Research Site New Haven Connecticut 06510 —
Research Site Clearwater Florida 33765 —
Research Site Jacksonville Florida 32204 —
Research Site Port Orange Florida 32127 —
Research Site Atlanta Georgia 30344 —
Research Site Decatur Georgia 30033 —
Research Site Springfield Illinois 62702 —
Research Site Munster Indiana 46321 —
Research Site Lexington Kentucky 40503 —
Research Site Detroit Michigan 48202 —
Research Site Rochester Minnesota 55905 —
Research Site Olive Branch Mississippi 38654 —
Research Site Kansas City Missouri 64111 —
Research Site Kansas City Missouri 64128 —
Research Site Kansas City Missouri 64151 —
Research Site Rosedale New York 11422 —
Research Site The Bronx New York 10455 —
Research Site Chapel Hill North Carolina 27599 —
Research Site New Bern North Carolina 28562 —
Research Site Toledo Ohio 43614 —
Research Site Grants Pass Oregon 97527 —
Research Site Bethlehem Pennsylvania 18017 —
Research Site Langhorne Pennsylvania 19047 —
Research Site East Providence Rhode Island 02914 —
Research Site Memphis Tennessee 38105 —
Research Site Brownsville Texas 78526 —
Research Site Corpus Christi Texas 78404 —
Research Site Houston Texas 77054 —
Research Site Sugar Land Texas 77479 —
Research Site Manassas Virginia 20110 —
Research Site Suffolk Virginia 23435 —
Research Site Madison Wisconsin 53792 —
Research Site Milwaukee Wisconsin 53295 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 220 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06034743, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 30, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06034743 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →