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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00330369
Other study ID # DAR-311
Secondary ID
Status Completed
Phase Phase 3
First received May 24, 2006
Last updated February 19, 2014
Start date June 2006
Est. completion date January 2009

Study information

Verified date February 2014
Source Gilead Sciences
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a research study of a new experimental drug called darusentan. Darusentan is not currently approved by the U.S. Food and Drug Administration (FDA) for use in the United States, which means that a doctor cannot prescribe this drug. The purpose of this study is to determine if darusentan is effective in reducing systolic blood pressure in subjects with resistant systolic hypertension, despite treatment with full doses of three or more antihypertensive drugs, including a diuretic.


Recruitment information / eligibility

Status Completed
Enrollment 352
Est. completion date January 2009
Est. primary completion date January 2009
Accepts healthy volunteers No
Gender Both
Age group 35 Years to 80 Years
Eligibility Inclusion Criteria:

- Subjects who are competent to provide written consent

- Aged 35 to 80 years

- Subjects with diabetes and/or chronic kidney disease must have a mean systolic blood pressure =130 mmHg

- All other subjects must have a mean systolic blood pressure =140 mmHg

- Receiving and adhering to full doses of appropriate guideline-recommended antihypertensive drugs from three different classes of antihypertensive agents, including a diuretic

- Female subjects of non-childbearing potential (i.e., post-menopausal for at lest 2 years; surgically sterile)

Exclusion Criteria:

- Average sitting systolic blood pressure =180 mmHg or diastolic blood pressure =110 mmHg

- Serum ALT or AST >2 x the upper limit of the normal range (ULN)

- Subjects who have experienced myocardial infarction, unstable angina pectoris, or a cerebrovascular accident (CVA) within 6 month; or sick sinus syndrome or second or third degree atrioventricular block, atrial fibrillation or recurrent atrial tachyarrhythmia, recurrent ventricular tachycardia, or symptomatic bradycardia

- Implanted pacemakers or implanted cardioverter defibrillator (ICD)

- Symptomatic congestive heart failure requiring treatment

- Hemodynamically significant valvular heart disease

- Type I diabetes mellitus

- Hemodialysis or peritoneal dialysis; or history of renal transplant

- Diagnosis or recurrence of malignancy within the past 3 years

- Sleep apnea, unless a recent sleep study demonstrates arterial oxygen saturation greater than or equal to 90%

- Subjects who perform alternating shift or night work

- Subjects who have participated in a clinical study involving another investigational drug or device within 4 weeks prior to Screening

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Darusentan
Darusentan administered orally once daily
Darusentan Placebo
Placebo to match darusentan administered orally once daily

Locations

Country Name City State
Argentina CIMEL Buenos Aires
Argentina DIM (Clinica Privada) Buenos Aires
Argentina Fundapres Buenos Aires
Argentina Hospital Britanico de Buenos Aires Buenos Aires
Argentina Hospital Jose Maria Ramos Meijia Buenos Aires
Argentina Hospital Municipal bernardo Houssay Buenos Aires
Argentina Medeos Buenos Aires
Argentina Sanatorio Municipal Dr. Julio Mendez Buenos Aires
Argentina Clinica Chutro SRL Cordoba
Argentina Hospital San Roque Cordoba
Brazil Hospital Governador Israel Pinheiro Belo Horizonte
Brazil Hospital Socor Belo Horizonte
Brazil Centro Medico de Campinas Campinas
Brazil Hospital de Clinicas da Universidade Federal do Parana Curitiba
Brazil Hospital das Clinicas Goiânia
Brazil Clinica de Exames Maceió
Brazil Instituto de Molestias São José do Rio Preto
Brazil Centro integrado hospital Sao Paulo
Brazil Centro Integrado Hospital do Rim e Hipertensao Sao Paulo
Brazil Hospital das Clinicas da Faculdade de Medicina da USP Sao Paulo
Canada Cambridge Cardiac Care Center Cambridge Ontario
Canada Clinical Research Solutions Kitchener Ontario
Denmark Hvidovre Hospital Hvidovre
Denmark Bispebjerg Hospital København
France CIC Hopital Jeanne D'Arc Dommartin les Toul
France CHU de Grenoble Grenoble Cedex
France CHU la Timone Service de cardiologie Marseille Cedex
France CHU Victor Provo Roubaix
France Hôpital Civil, Service HTA maladies vasculaires Strasbourg Cedex
Germany Kerckhoff-Klinik Forschungs GmbH Bad Nauheim
Germany Charité Campus Buch Berlin
Germany St Josefs-Hospital Cloppenburg
Germany Medizinische Hochschule Hannover Hannover
Germany Universitätsklinikum Schleswig-Holstein Lübeck
Italy Azienda Ospedaliera University of Padua Policlinico Padua
Spain Fundacio Puigvert Barcelona
Spain Hospital Clinic i Provincial Barcelona
Spain Hospital del Mar Barcelona
Spain Hospital Universitario de Santiago Coruña
Spain Hospital Clínico San Cecilio Granada
Spain Hospital Clínico de San Carlos Madrid
Spain Hospital Universitario 12 de Octobre Madrid
Spain Hospital Carlos Haya Malaga
Sweden Cardiovascular Research, Karolinska Institue Stockholm
United Kingdom Stonehill Medical Centre Bolton,
United Kingdom Townhead Surgery Scotland
United Kingdom Avenue Surgery Wiltshire
United Kingdom Hathaway Medical Centre Wiltshire
United States Northeast Clinical Research Centers, Inc. Allentown Pennsylvania
United States Maine Research Associates Auburn Maine
United States MODEL Clinical Research Baltimore Maryland
United States Professional Clinical Research Benzonia Michigan
United States UAB Hypertension Program Birmingham Alabama
United States Connecticut Clinical Research, LLC Bridgeport Connecticut
United States Bronx VA Medical Center / Mt. Sinai Bronx New York
United States Burke Internal Medicine, Inc. Burke Virginia
United States Global Research Partners Calhoun Georgia
United States Heritage Cardiology Associates Camp Hill Pennsylvania
United States CAMC Clinical Trials Center Charleston West Virginia
United States The Lindner Clinical Trial Center Cincinnati Ohio
United States Neem Research Group, Inc. Columbia South Carolina
United States Deerfield Beach Cardiology Associates Deerfield Beach Florida
United States Complete Renal Care Denver Colorado
United States Internal Medicine & Industrial Medicine Desoto Texas
United States Brandywine Clinical Research Downingtown Pennsylvania
United States Chicago Heart & Vein Clinic Elk Grove Village Illinois
United States Evanston Northwestern Healthcare Evanston Illinois
United States West Coast Cardiology Associates Fairview Park Ohio
United States Nephrology and Hypertension / Hurley Medical Center Flint Michigan
United States White-Wilson Medical Center Fort Walton Beach Florida
United States T&R Clinical, P.A. Ft Worth Texas
United States AMK Research Gainsville Florida
United States Peninsula Inernal Medicine Gig Harbor Washington
United States Physicians East, PA Greenville North Carolina
United States Clinical Investigation Specialists, Inc. Gurnee Illinois
United States A.G.A. Clinical Trials Hialeah Florida
United States Hillsboro Cardiology, PC Hillsboro Oregon
United States Kula Research Honolulu Hawaii
United States Chrishard Medical Group Inglewood California
United States Professional Clinical Research Interlochen Michigan
United States Jacksonville Center for Clinical Jacksonville Florida
United States Ricardo A. Bedoya, Cardiology Jupiter Florida
United States Green and Seidner Family Practice Associates Lansdale Pennsylvania
United States Pri-Med Care Lewisville Texas
United States Midwest Heart Foundation Lombard Illinois
United States VA Medical Center - WLA Los Angeles California
United States Texas Tech University Health Sciences Center Lubbock Texas
United States Manassas Clinical Research Center Manassas Virginia
United States American Clinical Research LLC Marrero Louisiana
United States International Research Association Miami Florida
United States Diabetes Center of the Southwest Midland Texas
United States Comprehensive Heart Failure Center Mobile Alabama
United States COR Clinical Research Oklahoma City Oklahoma
United States Sooner Clinical Research Oklahoma City Oklahoma
United States Southwest Cardiology Associates Oklahoma City Oklahoma
United States Maryland Medical Research/Og Medical Center Oxon Hill Maryland
United States Specialty Medical Center Pahrump Nevada
United States Temple University Hospital Philadelphia Pennsylvania
United States The Bracane Company Plano Texas
United States RI Hospital Providence Rhode Island
United States Clinical Associates Reisterstown Maryland
United States McGuire VA Medical Center Richmond Virginia
United States Rockville Internal Medicine Group Rockville Maryland
United States Sacramento Heart and Vascular Sacramento California
United States Innovative Clinical Trials San Antonio Texas
United States Apex Research Institute Santa Ana California
United States Cardiovascular Center of Sarasota Sarasota Florida
United States Cardiovascular Consultants of Maine Scarborough Maine
United States Medical Research Institute Slidell Louisiana
United States Liberty Research Center Tacoma Washington
United States Tampa Bay Nephrology Tampa Florida
United States Canyon Clinical Research Tucson Arizona
United States Castlerock Clinical Research Consultants Tulsa Oklahoma
United States MedStar Diabetes Institute at Washington Hospital Center Washington District of Columbia
United States Metabolic Research Institute, Inc. West Palm Beach Florida

Sponsors (1)

Lead Sponsor Collaborator
Gilead Sciences

Countries where clinical trial is conducted

United States,  Argentina,  Brazil,  Canada,  Denmark,  France,  Germany,  Italy,  Spain,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in trough sitting systolic and diastolic blood pressure measured by sphygmomanometry Baseline to Week 14 No
Secondary Change from baseline in mean 24-hour systolic and diastolic ambulatory blood pressure Baseline to Week 14 No
Secondary Percentage of subjects to reach systolic blood pressure goal Week 14 No
Secondary Change from baseline in estimated glomerular filtration rate (eGFR) Baseline to Week 14 No
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