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Generated: December 15, 2018

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CLINICAL TRIALS PROFILE FOR NORVASC

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Clinical Trials for Norvasc

Trial ID Title Status Sponsor Phase Summary
NCT00125463 Candesartan Antihypertensive Survival Evaluation in Japan (CASE-J) Trial of Cardiovascular Events in High-Risk Hypertensive Patients Unknown status The Japanese Society of Hypertension Phase 3 The purpose of this study is to compare an angiotensin II receptor antagonist (candesartan cilexetil– Blopress®) and a calcium channel blocker (amlodipine besilate– Norvasc®/Amlodin®) in terms of the incidence of cardiovascular events among high-risk hypertensive patients.
NCT00281580 Telmisartan (Micardis) and Amlodipine (Norvasc) - Factorial Design Study for the Treatment of Hypertension Completed Boehringer Ingelheim Phase 3 To demonstrate that Micardis and Norvasc when used together are more effective at lowering blood pre ssure.
NCT00294567 Azelnidipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients by Serial Volumetric IVUS Analysis(ALPS-J) Completed Japan Heart Foundation Phase 4 In patients with hypertension who undergo elective PCI, the effects of long-term administration of Calblock (azelnidipine) on plaque volume will be determined quantitatively by 3D-IVUS and compared with those of amlodipine besilate (Norvasc or Amlodin).
NCT00294567 Azelnidipine Anti-Coronary Atherosclerotic Trial in Hypertensive Patients by Serial Volumetric IVUS Analysis(ALPS-J) Completed Juntendo University Hospital Phase 4 In patients with hypertension who undergo elective PCI, the effects of long-term administration of Calblock (azelnidipine) on plaque volume will be determined quantitatively by 3D-IVUS and compared with those of amlodipine besilate (Norvasc or Amlodin).
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.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Norvasc

Condition Name

Condition Name for Norvasc
Intervention Trials
Hypertension 27
Healthy 12
Chronic Stable Angina 2
Vasospastic Angina 2
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Condition MeSH

Condition MeSH for Norvasc
Intervention Trials
Hypertension 22
Coronary Artery Disease 3
Angina Pectoris, Variant 3
Myocardial Ischemia 3
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Clinical Trial Locations for Norvasc

Trials by Country

Trials by Country for Norvasc
Location Trials
United States 146
United Kingdom 9
Canada 7
China 4
Germany 3
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Trials by US State

Trials by US State for Norvasc
Location Trials
Texas 10
North Carolina 7
Florida 7
Missouri 6
Indiana 5
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Clinical Trial Progress for Norvasc

Clinical Trial Phase

Clinical Trial Phase for Norvasc
Clinical Trial Phase Trials
Phase 4 17
Phase 3 9
Phase 2 2
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Clinical Trial Status

Clinical Trial Status for Norvasc
Clinical Trial Phase Trials
Completed 37
Recruiting 5
Not yet recruiting 3
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Clinical Trial Sponsors for Norvasc

Sponsor Name

Sponsor Name for Norvasc
Sponsor Trials
Boehringer Ingelheim 3
Pfizer 3
Daiichi Sankyo Inc. 3
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Sponsor Type

Sponsor Type for Norvasc
Sponsor Trials
Other 52
Industry 31
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