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Last Updated: November 24, 2024

CLINICAL TRIALS PROFILE FOR CANDESARTAN CILEXETIL


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All Clinical Trials for candesartan cilexetil

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00108706 ↗ Acute Candesartan Cilexetil Outcomes Stroke Trial (ACCOST) Unknown status Takeda Phase 4 2004-12-01 The aim of this study is to determine whether it is safe and effective to give the Angiotensin Receptor Blocker (ARB) Candesartan within the first 72 hours following acute stroke.
NCT00108706 ↗ Acute Candesartan Cilexetil Outcomes Stroke Trial (ACCOST) Unknown status City Hospitals Sunderland NHS Foundation Trust Phase 4 2004-12-01 The aim of this study is to determine whether it is safe and effective to give the Angiotensin Receptor Blocker (ARB) Candesartan within the first 72 hours following acute stroke.
NCT00120003 ↗ Scandinavian Candesartan Acute Stroke Trial (SCAST) Completed AstraZeneca Phase 3 2005-06-01 The purpose of this trial is to assess whether the blood pressure lowering agent candesartan (an angiotensin receptor type 1 blocker) is effective when given to patients with acute stroke and elevated blood pressure. Hypothesis: AT1 receptor blockade with candesartan in acute stroke will: 1. reduce the risk of death or major disability at 6 months by a 6% absolute risk reduction, relative to placebo. 2. reduce the risk of the combined event of "vascular" death, myocardial infarction, or stroke during the first 6 months by a 25% relative risk reduction, relative to placebo
NCT00120003 ↗ Scandinavian Candesartan Acute Stroke Trial (SCAST) Completed Southern-Eastern Norway Health Authorities RHF Phase 3 2005-06-01 The purpose of this trial is to assess whether the blood pressure lowering agent candesartan (an angiotensin receptor type 1 blocker) is effective when given to patients with acute stroke and elevated blood pressure. Hypothesis: AT1 receptor blockade with candesartan in acute stroke will: 1. reduce the risk of death or major disability at 6 months by a 6% absolute risk reduction, relative to placebo. 2. reduce the risk of the combined event of "vascular" death, myocardial infarction, or stroke during the first 6 months by a 25% relative risk reduction, relative to placebo
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for candesartan cilexetil

Condition Name

Condition Name for candesartan cilexetil
Intervention Trials
Hypertension 30
Essential Hypertension 5
Healthy 4
Stroke 2
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Condition MeSH

Condition MeSH for candesartan cilexetil
Intervention Trials
Hypertension 40
Essential Hypertension 10
Heart Failure 4
Stroke 4
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Clinical Trial Locations for candesartan cilexetil

Trials by Country

Trials by Country for candesartan cilexetil
Location Trials
United States 102
Japan 32
Korea, Republic of 22
China 17
Germany 14
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Trials by US State

Trials by US State for candesartan cilexetil
Location Trials
California 7
Texas 5
Ohio 5
North Carolina 5
Florida 5
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Clinical Trial Progress for candesartan cilexetil

Clinical Trial Phase

Clinical Trial Phase for candesartan cilexetil
Clinical Trial Phase Trials
Phase 4 12
Phase 3 26
Phase 2/Phase 3 1
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Clinical Trial Status

Clinical Trial Status for candesartan cilexetil
Clinical Trial Phase Trials
Completed 47
Unknown status 12
Withdrawn 4
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Clinical Trial Sponsors for candesartan cilexetil

Sponsor Name

Sponsor Name for candesartan cilexetil
Sponsor Trials
AstraZeneca 23
Takeda 14
CJ HealthCare Corporation 7
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Sponsor Type

Sponsor Type for candesartan cilexetil
Sponsor Trials
Industry 71
Other 43
NIH 1
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