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Completed Phase 3 Interventional Results available

One-Year Safety and Tolerability Study of Azilsartan Medoxomil in Participants With Essential Hypertension

ClinicalTrials.gov ID: NCT00695955

Public ClinicalTrials.gov record NCT00695955. 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 May 17, 2026, 1:45 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 One-Year Phase 3, Open-Label Study to Evaluate the Safety and Tolerability of TAK-491 in Subjects With Essential Hypertension

Study identification

NCT ID
NCT00695955
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
669 participants

Conditions and interventions

Conditions

Interventions

  • Azilsartan medoxomil with or without add-on chlorthalidone Drug
  • Azilsartan medoxomil with or without add-on hydrochlorothiazide Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
May 31, 2007
Primary completion
Apr 30, 2010
Completion
Apr 30, 2010
Last update posted
Apr 18, 2011

2007 – 2010

United States locations

U.S. sites
39
U.S. states
18
U.S. cities
39
Facility City State ZIP Site status
Not listed Ozark Alabama
Not listed Tallassee Alabama
Not listed Long Beach California
Not listed Santa Rosa California
Not listed Spring Valley California
Not listed Colorado Springs Colorado
Not listed Trumbull Connecticut
Not listed Waterbury Connecticut
Not listed Fort Lauderdale Florida
Not listed Hollywood Florida
Not listed Jacksonville Florida
Not listed Miami Florida
Not listed Pembroke Pines Florida
Not listed Pinellas Park Florida
Not listed Atlanta Georgia
Not listed Augusta Georgia
Not listed Brooklyn Center Minnesota
Not listed Olive Branch Mississippi
Not listed Rochester New York
Not listed Charlotte North Carolina
Not listed Raleigh North Carolina
Not listed Salisbury North Carolina
Not listed Winston-Salem North Carolina
Not listed Akron Ohio
Not listed Cincinnati Ohio
Not listed Mogadore Ohio
Not listed Springdale Ohio
Not listed Oklahoma City Oklahoma
Not listed Philadelphia Pennsylvania
Not listed Anderson South Carolina
Not listed Mt. Pleasant South Carolina
Not listed Simpsonville South Carolina
Not listed Bristol Tennessee
Not listed Nashville Tennessee
Not listed Arlington Texas
Not listed Austin Texas
Not listed North Richland Hills Texas
Not listed Salt Lake City Utah
Not listed Norfolk Virginia

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00695955, 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 18, 2011 · Synced May 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00695955 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →