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Generated: September 16, 2019

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CLINICAL TRIALS PROFILE FOR CADUET

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Clinical Trials for Caduet

Trial ID Title Status Sponsor Phase Summary
NCT00150384 Clinical Utility of Caduet in Achieving Blood Pressure and Lipid Endpoints in a Specific Patient Population Completed Pfizer Phase 4 The purpose is to demonstrate the utility of Caduet (amlodipine/atorvastatin) in the African American population
NCT00332761 Caduet in an Untreated Subject Population Completed Pfizer Phase 4 The purpose of this study is to determine if Caduet will lower blood pressure to <140/90 mmHg and lower LDL Cholesterol to <100 mg/dL in subjects with hypertension and dyslipidemia who are not currently being treated for these medical conditions.
NCT00407537 Caduet vs Usual Care in Subjects With Hypertension and Additional Risk Factors Completed Pfizer Phase 4 To investigate whether a Caduet based treatment strategy might result in greater reduction in total cardiovascular risk as compared to usual care in subjects with hypertension and additional risk factors.
NCT00412113 A Multi-Risk Factor Strategy vs a Guideline-Based Approach in Achieving Blood Pressure and Lipid Goals in Hypertensives at Extra Risk Completed Pfizer Phase 4 The purpose of this study is to investigate whether an aggressive multi-risk factor management strategy (Caduet plus therapeutic lifestyle changes (TLC) regimen) will result in greater percentage of patients achieving blood pressure and low density lipoprotein cholesterol (LDL-C) goals compared with a Joint National Committee 7/ National Cholesterol Education Program Adult Treatment Panel III (JNC 7/NCEP ATP III) guideline-based approach (Norvasc plus TLC regimen) after 6 weeks of treatment in primary prevention subjects with hypertension and additional risk factors, including dyslipidemia.
NCT00579254 Real Life Experience With Caduet In Patients With Cardiovascular Risk Factors Terminated Pfizer Phase 4 To assess the effect of single pill therapy on the management of hypertension and other cardiovascular risk factors (e.g., dyslipidemia) in Indian patients in whom the treating doctor has already considered that the administration of the amlodipine/atorvastatin single pill to be appropriate
NCT01107743 Amlodipine/Atorvastatin (Caduet®) Drug Use Investigation (Regulatory Post Marketing Commitment Plan) Completed Pfizer N/A In this survey, to collect the safety and efficacy information of Amlodipine /Atorvastatin (Caduet® Combination Tablets) in daily medical practice will be examined. In addition, the necessity of special Investigation and post-marketing clinical studies will be examined, while investigating unexpected adverse drug reactions during the survey period and understanding of the status of frequency of adverse drug reactions in daily medical practice.
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Clinical Trial Conditions for Caduet

Condition Name

Condition Name for Caduet
Intervention Trials
Hypertension 7
Hypercholesterolemia 3
Dyslipidemia 3
Angina Pectoris 2
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Condition MeSH

Condition MeSH for Caduet
Intervention Trials
Hypertension 4
Dyslipidemias 4
Hypercholesterolemia 3
Angina Pectoris 2
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Clinical Trial Locations for Caduet

Trials by Country

Trials by Country for Caduet
Location Trials
United States 66
Japan 8
Mexico 4
Venezuela 3
Korea, Republic of 3
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Trials by US State

Trials by US State for Caduet
Location Trials
Virginia 3
Tennessee 3
Pennsylvania 3
Ohio 3
New York 3
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Clinical Trial Progress for Caduet

Clinical Trial Phase

Clinical Trial Phase for Caduet
Clinical Trial Phase Trials
Phase 4 10
Phase 1 2
N/A 1
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Clinical Trial Status

Clinical Trial Status for Caduet
Clinical Trial Phase Trials
Completed 9
Not yet recruiting 2
Terminated 1
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Clinical Trial Sponsors for Caduet

Sponsor Name

Sponsor Name for Caduet
Sponsor Trials
Pfizer 8
Dr. Reddy's Laboratories Limited 2
The University of Texas Medical Branch, Galveston 1
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Sponsor Type

Sponsor Type for Caduet
Sponsor Trials
Industry 10
Other 5
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