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Last Updated: December 22, 2024

CLINICAL TRIALS PROFILE FOR MICARDIS


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All Clinical Trials for micardis

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00034840 ↗ Telmisartan vs. Valsartan in Patients With Mild to Moderate Hypertension Following a Missed Dose Completed Bayer Phase 4 2001-10-01 The primary objectives are to demonstrate that MICARDIS® (telmisartan) is statistically superior to Diovan® (valsartan) in reducing diastolic blood pressure (DBP) following a missed dose at the end of a 6 to 8-week treatment period as measured by the 24-hour ABPM mean and to demonstrate that MICARDIS® is statistically superior to Diovan® in reducing DBP during the last 6-hours of the 24-hour dosing interval as measured by ABPM following a dose of active study medication at the end of a 6 to 8-week treatment period.
NCT00034840 ↗ Telmisartan vs. Valsartan in Patients With Mild to Moderate Hypertension Following a Missed Dose Completed GlaxoSmithKline Phase 4 2001-10-01 The primary objectives are to demonstrate that MICARDIS® (telmisartan) is statistically superior to Diovan® (valsartan) in reducing diastolic blood pressure (DBP) following a missed dose at the end of a 6 to 8-week treatment period as measured by the 24-hour ABPM mean and to demonstrate that MICARDIS® is statistically superior to Diovan® in reducing DBP during the last 6-hours of the 24-hour dosing interval as measured by ABPM following a dose of active study medication at the end of a 6 to 8-week treatment period.
NCT00034840 ↗ Telmisartan vs. Valsartan in Patients With Mild to Moderate Hypertension Following a Missed Dose Completed Boehringer Ingelheim Phase 4 2001-10-01 The primary objectives are to demonstrate that MICARDIS® (telmisartan) is statistically superior to Diovan® (valsartan) in reducing diastolic blood pressure (DBP) following a missed dose at the end of a 6 to 8-week treatment period as measured by the 24-hour ABPM mean and to demonstrate that MICARDIS® is statistically superior to Diovan® in reducing DBP during the last 6-hours of the 24-hour dosing interval as measured by ABPM following a dose of active study medication at the end of a 6 to 8-week treatment period.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for micardis

Condition Name

Condition Name for micardis
Intervention Trials
Hypertension 53
Healthy 3
Alzheimer's Disease 2
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Condition MeSH

Condition MeSH for micardis
Intervention Trials
Hypertension 50
Essential Hypertension 6
Kidney Diseases 3
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Clinical Trial Locations for micardis

Trials by Country

Trials by Country for micardis
Location Trials
United States 271
Canada 45
Korea, Republic of 9
Australia 7
France 6
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Trials by US State

Trials by US State for micardis
Location Trials
California 12
Illinois 11
Texas 10
Georgia 10
Pennsylvania 9
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Clinical Trial Progress for micardis

Clinical Trial Phase

Clinical Trial Phase for micardis
Clinical Trial Phase Trials
Phase 4 18
Phase 3 12
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for micardis
Clinical Trial Phase Trials
Completed 61
Recruiting 7
Active, not recruiting 2
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Clinical Trial Sponsors for micardis

Sponsor Name

Sponsor Name for micardis
Sponsor Trials
Boehringer Ingelheim 52
Bayer 3
HK inno.N Corporation 2
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Sponsor Type

Sponsor Type for micardis
Sponsor Trials
Industry 66
Other 33
NIH 1
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