Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
31,654
archived clinical trials in
Cardiology

Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Santa Monica, CA
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #4
mi
from
Santa Monica, CA
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Coral Gables, FL
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #5
mi
from
Coral Gables, FL
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Tampa, FL
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #6
mi
from
Tampa, FL
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
West Palm Beach, FL
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #7
mi
from
West Palm Beach, FL
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Alpharetta, GA
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #8
mi
from
Alpharetta, GA
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
New York, NY
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #9
mi
from
New York, NY
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Franklin, TN
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #10
mi
from
Franklin, TN
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Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
Safety and Effectiveness of EN3835 in the Treatment of EFP in Women
A Phase 2 Open-Label Study of EN3835 In The Treatment of Edematous Fibrosclerotic Panniculopathy
Status: Enrolling
Updated: 12/31/1969
Endo Clinical Trial Site #11
mi
from
Austin, TX
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The Effects of Traditional Acupuncture on Mechanisms of Coronary Heart Disease
The Effects of Traditional Acupuncture on Mechanisms of Coronary Heart Disease
Status: Enrolling
Updated:  12/31/1969
mi
from
Los Angeles, CA
The Effects of Traditional Acupuncture on Mechanisms of Coronary Heart Disease
The Effects of Traditional Acupuncture on Mechanisms of Coronary Heart Disease
Status: Enrolling
Updated: 12/31/1969
Cedars-Sinai Women's Heart Center
mi
from
Los Angeles, CA
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Reproductive Hormones And Pre-Clinical Cardiovascular Disease (CVD) In Women
Reproductive Hormones And Pre-Clinical CVD In Women
Status: Enrolling
Updated:  12/31/1969
mi
from
Los Angeles, CA
Reproductive Hormones And Pre-Clinical Cardiovascular Disease (CVD) In Women
Reproductive Hormones And Pre-Clinical CVD In Women
Status: Enrolling
Updated: 12/31/1969
Cedars-Sinai Medical Center
mi
from
Los Angeles, CA
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Platelet and Tissue cAMP: Novel Biomarkers of Milrinone Efficacy in Children
Platelet and Tissue cAMP: Novel Biomarkers of Milrinone Efficacy in Children
Status: Enrolling
Updated:  12/31/1969
mi
from
Aurora, CO
Platelet and Tissue cAMP: Novel Biomarkers of Milrinone Efficacy in Children
Platelet and Tissue cAMP: Novel Biomarkers of Milrinone Efficacy in Children
Status: Enrolling
Updated: 12/31/1969
Children's Hospital Colorado
mi
from
Aurora, CO
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The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia
The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia
The Effects of Prolonged Standing Compared to Prolonged Sitting on Postprandial Lipemia
Status: Enrolling
Updated: 12/31/1969
University of Texas at Austin Human Performance Laboratory
mi
from
Austin, TX
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The Effect of Sitting and Moderate Exercise on Plasma Triglyceride Elevation After a Meal
The Effect of Sitting and Moderate Exercise on Plasma Triglyceride Elevation After a Meal
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
The Effect of Sitting and Moderate Exercise on Plasma Triglyceride Elevation After a Meal
The Effect of Sitting and Moderate Exercise on Plasma Triglyceride Elevation After a Meal
Status: Enrolling
Updated: 12/31/1969
University of Texas at Austin Human Performance Laboratory
mi
from
Austin, TX
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Prolonged Sitting on Responses to Short-Term Exercise Training
Effect of Prolonged Sitting on Metabolic and Cardiovascular Responses to Short-Term Exercise Training
Status: Enrolling
Updated:  12/31/1969
mi
from
Austin, TX
Prolonged Sitting on Responses to Short-Term Exercise Training
Effect of Prolonged Sitting on Metabolic and Cardiovascular Responses to Short-Term Exercise Training
Status: Enrolling
Updated: 12/31/1969
University of Texas at Austin Human Performance Laboratory
mi
from
Austin, TX
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
New Haven, CT
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Yale-New Haven Hospital
mi
from
New Haven, CT
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Ann Arbor, MI
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
University of Michigan Health Systems
mi
from
Ann Arbor, MI
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Grand Rapids, MI
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Spectrum Health Hospitals
mi
from
Grand Rapids, MI
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
New York, NY
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
New York Langone Medical Center
mi
from
New York, NY
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Roslyn, NY
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
St. Francis Hospital
mi
from
Roslyn, NY
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Columbus, OH
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Riverside Methodist Hospital
mi
from
Columbus, OH
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Harrisburg, PA
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Pinnacle Health/Moffitt Heart and Vascular Institute
mi
from
Harrisburg, PA
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Dallas, TX
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Baylor Heart and Vascular Hospital
mi
from
Dallas, TX
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Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated:  12/31/1969
mi
from
Milwaukee, WI
Medtronic CoreValve Evolut R U.S. Clinical Study (Evolut 34R Addendum)
Medtronic CoreValve Evolut R United States Clinical Study (Evolut 34R Addendum)
Status: Enrolling
Updated: 12/31/1969
Aurora Health Care, St. Luke's Medical Center
mi
from
Milwaukee, WI
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Boston, MA
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Brigham and Women's Hosp
mi
from
Boston, MA
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Nagoya-shi,
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Local Institution
mi
from
Nagoya-shi,
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Falls Church, VA
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Inova Heart and Vascular Institute
mi
from
Falls Church, VA
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Chicago, IL
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Northwestern Medicine
mi
from
Chicago, IL
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Tustin, CA
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Orange County Research Center
mi
from
Tustin, CA
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Durham, NC
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Duke Advanced Heart and Lung Failure Clinic
mi
from
Durham, NC
Click here to add this to my saved trials
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated:  12/31/1969
mi
from
Indianapolis, IN
A Study of Continuous Infusions of HNO (Nitroxyl) Donor in Patients With Heart Failure and Impaired Systolic Function
A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients With Heart Failure and Impaired Systolic Function
Status: Enrolling
Updated: 12/31/1969
Indiana University School of Medicine
mi
from
Indianapolis, IN
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Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated:  12/31/1969
mi
from
Anniston, AL
Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Anniston, AL
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Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated:  12/31/1969
mi
from
Jacksonville, FL
Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Jacksonville, FL
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Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated:  12/31/1969
mi
from
Port Orange, FL
Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Port Orange, FL
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Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated:  12/31/1969
mi
from
Cincinnati, OH
Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
A Phase 2a Randomized, Blinded, Placebo-controlled Study to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Ascending Doses of MEDI6012 in Subjects With Stable Atherosclerotic Cardiovascular Disease
Status: Enrolling
Updated: 12/31/1969
Clinical Research Facility
mi
from
Cincinnati, OH
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Apple Heart Study: Assessment of Wristwatch-Based Photoplethysmography to Identify Cardiac Arrhythmias
Apple Heart Study: Assessment of Wristwatch-Based Photoplethysmography to Identify Cardiac Arrhythmias
Status: Enrolling
Updated:  12/31/1969
mi
from
Stanford, CA
Apple Heart Study: Assessment of Wristwatch-Based Photoplethysmography to Identify Cardiac Arrhythmias
Apple Heart Study: Assessment of Wristwatch-Based Photoplethysmography to Identify Cardiac Arrhythmias
Status: Enrolling
Updated: 12/31/1969
Stanford University
mi
from
Stanford, CA
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Pasadena, CA
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Foothill Cardiology
mi
from
Pasadena, CA
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Coral Springs, FL
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Holy Cross Medical Group
mi
from
Coral Springs, FL
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Port Charlotte, FL
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Charlotte Heart Group
mi
from
Port Charlotte, FL
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Atlanta, GA
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Atlanta Institute For Medical Research, Inc
mi
from
Atlanta, GA
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Cumming, GA
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Atlanta Heart Specialists, LLC
mi
from
Cumming, GA
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Munster, IN
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Cardiovascular Research of Northwest Indiana, LLC
mi
from
Munster, IN
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Owensboro, KY
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Research Integrity, Llc
mi
from
Owensboro, KY
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
New Orleans, LA
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Ochsner Health System
mi
from
New Orleans, LA
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Rockport, ME
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Penobscot Bay Medical Center
mi
from
Rockport, ME
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Alpena, MI
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Endeavor Medical Research
mi
from
Alpena, MI
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Saint Joseph, MI
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Great Lakes Heart and Vascular Institute PC
mi
from
Saint Joseph, MI
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Saint Paul, MN
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
HealthEast Medical Research Institute
mi
from
Saint Paul, MN
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Jackson, MS
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Jackson Heart Clinic
mi
from
Jackson, MS
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Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated:  12/31/1969
mi
from
Elmer, NJ
Eliminate Thromboembolism: Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Eliminate Thromboembolism (ELITE): Improving Anticoagulation in Non-valvular Atrial Fibrillation Patients
Status: Enrolling
Updated: 12/31/1969
Cardiovascular Associates of the Delaware Valley
mi
from
Elmer, NJ
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