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The following trials provide information to treat various types of cardiovascular diseases, both for ongoing and completed clinical trials. For more information on this therapy area please click here.
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A Study in Healthy Volunteers to Assess the Tolerability and Blood Levels of a Single Dose of AZD7687
- Study Id
- D2710C00001
- Disease
- diabetes mellitus
- Drug Name
- AZD7687
- Study Name
- D2710C00001
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Apr 26, 2011
- D2710C00001.pdf (135 KB)
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A randomised, single-blind, placebo-controlled, two-centre phase I study in healthy volunteers to assess the safety, tolerability and pharmacokinetics of AZD8329 after single ascending oral doses
- Study Id
- D2350C00001
- Disease
- diabetes mellitus
- Drug Name
- AZD8329
- Study Name
- D2350C00001
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Feb 23, 2011
- D2350C00001.pdf (43 KB)
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A Phase I, Single Centre, Single-blind, Randomised, Placebo-controlled, Parallel-group Study to Assess the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of oral AZD8329 after Administration of Multiple Ascending Doses in Abdominally Obese but otherwise Healthy Male Subjects
- Study Id
- D2350C00010
- Disease
- obesity
- Drug Name
- AZD8329
- Study Name
- D2350C00010
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Aug 17, 2011
- D2350C00010.pdf (215 KB)
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A sequential, open label study to compare the pharmacokinetics,safety and tolerability of Ticagrelor and Venlafaxine given concomitantly in healthy subjects aged 18 to 45 years.
- Study Id
- D5130C00073
- Drug Name
- Brilinta
- Study Name
- D5130C00073
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Jul 9, 2012
- D5130C00073.pdf (174 KB)
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PATTERN OF STATINS USE IN CATALONIA
- Study Id
- NIS-CES-CRE-2011/1
- Disease
- cardiovascular diseases
- Drug Name
- Crestor
- Study Name
- NIS-CES-CRE-2011/1
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Mar 21, 2012
- NIS-CES-CRE-2011-1.pdf (151 KB)
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Bioequivalence Study of the Fixed-dose Combination of Saxagliptin/Metformin XR Tablets Relative to Saxagliptin (Onglyza™ ) Tablets and Australia-sourced Diabex XR Tablets Coadministered to Healthy Subjects in the Fed State During Steady-state Administration
- Study Id
- D1681C00004
- Disease
- cardiovascular and blood physiology
- Drug Name
- Onglyza
- Study Name
- D1681C00004
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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May 23, 2012
- D1681C00004.pdf (119 KB)
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A 24-week, multicentre, randomised, double-blind,age-stratified, placebo controlled phase III study with an 80-week extension period to evaluate the efficacy and safety of dapagliflozin 10 mg /day in patients with T2DM and cardiovascular disease, who exhibit inadequate glycaemic control on usual care
- Study Id
- D1690C00019
- Disease
- diabetes mellitus
- Drug Name
- dapagliflozin
- Study Name
- D1690C00019
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
-
Oct 13, 2011
- D1690C00019.pdf (197 KB)
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A 24-week, multicentre, randomised, double-blind, age-stratified, placebo controlled, phase III study with a 80-week extension period to evaluate the efficacy and safety of dapagliflozin 10 mg/day in pts with T2DM, CV disease and hypertension who exhibit inadequate glycaemic control on usual care
- Study Id
- D1690C00018
- Disease
- diabetes mellitus
- Drug Name
- dapagliflozin
- Study Name
- D1690C00018
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
-
Oct 13, 2011
- D1690C00018.pdf (176 KB)
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A 24-week,Multicentre,Randomised,Double-Blind,Placebo-Contr,Parallel-Group,International Phase III Study with 24week Extension to Evaluate the Safety and Efficacy of Dapagliflozin 10 mg/Day in patients with Type 2 Diabetes who have Inadequate Glyc Control on a DPP-4 inhibitor Sitagliptin+/-Metformin
- Study Id
- D1690C00010
- Disease
- diabetes mellitus
- Drug Name
- dapagliflozin
- Study Name
- D1690C00010
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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May 28, 2012
- D1690C00010.pdf (199 KB)
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A 24-week international, randomized, parallel-group, double-blind, placebo-controlled Phase III study with a 24-week extension period to evaluate the efficacy and safety of dapagliflozin therapy when added to the therapy of patients with type 2 diabetes with inadequate glycaemic control on insulin
- Study Id
- D1690C00006
- Disease
- diabetes mellitus
- Drug Name
- dapagliflozin
- Study Name
- D1690C00006
- Recruiting Status
- Closed
- Protocol Status
- Not Available
- Report
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Sep 16, 2010
- D1690C00006.pdf (144 KB)
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