A Study to Assess Efficacy and Safety of Baxdrostat in Participants With Primary Aldosteronism

ClinicalTrials.gov ID: NCT07007793

Public ClinicalTrials.gov record NCT07007793. 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.

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ClinicalTrials.gov public records Last synced Apr 22, 2026, 8:30 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 Adult Participants With Primary Aldosteronism

Study identification

NCT ID: NCT07007793
Recruitment status: Recruiting
Study type: Interventional
Phase: Phase 3
Lead sponsor: AstraZeneca; Industry
Enrollment: 250 participants

Conditions and interventions

Conditions

Primary Hyperaldosteronism

Interventions

Baxdrostat Drug
Placebo Drug

Drug

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Not listed

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

Study timeline

Start date: Aug 6, 2025
Primary completion: Feb 17, 2028
Completion: Feb 17, 2028
Last update posted: Apr 19, 2026

2025 – 2028

United States locations

U.S. sites: 21
U.S. states: 15
U.S. cities: 20

Facility	City	State	ZIP	Site status
Research Site	Los Angeles	California	90048	Not yet recruiting
Research Site	San Francisco	California	94110	Not yet recruiting
Research Site	Farmington	Connecticut	06030	Not yet recruiting
Research Site	Chicago	Illinois	60611	Not yet recruiting
Research Site	Springfield	Illinois	62702	Recruiting
Research Site	Baltimore	Maryland	21287	Not yet recruiting
Research Site	Boston	Massachusetts	02111	Recruiting
Research Site	Boston	Massachusetts	02115	Recruiting
Research Site	Ann Arbor	Michigan	48109	Recruiting
Research Site	Rochester	Minnesota	55902	Recruiting
Research Site	Olive Branch	Mississippi	38654	Recruiting
Research Site	Kansas City	Missouri	64151	Withdrawn
Research Site	New York	New York	10065	Not yet recruiting
Research Site	Cleveland	Ohio	44195	Not yet recruiting
Research Site	Columbus	Ohio	43210	Recruiting
Research Site	Portland	Oregon	97239	Withdrawn
Research Site	Bethlehem	Pennsylvania	18017	Recruiting
Research Site	Philadelphia	Pennsylvania	19104	Not yet recruiting
Research Site	Columbia	South Carolina	29203	Recruiting
Research Site	Brownsville	Texas	78526	Withdrawn
Research Site	Dallas	Texas	75390	Recruiting

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 68 non-U.S. sites.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT07007793, 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 Apr 19, 2026 · Synced Apr 22, 2026

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The complete protocol, eligibility criteria, and contact information for NCT07007793 live on ClinicalTrials.gov.

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