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  • Cardiovascular

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.

There are a number of ways to help you find trial information.  By using these filters you can find (i) recruiting status, (ii) therapy area, (iii) product and/or (iv) phase of drug development.  You can use one or all filters to identify your specific needs.

When a trial completes the results are reported here no later than one year after completion – this is why you may sometimes find that a Report is unavailable when you are searching through ‘closed’ trials.

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  • collapse Compliance of Patients With Essential Hypertension Treated With Candesartan or Candesartan/Hydrochlorothiazide
  • collapse Pan-European Survey on the Under Treatment of Hypercholesterolemia
  • collapse An observational study into the usage and efficacy of Crestor 5mg as a start dosage in achieving the LDL-C target level in both statin-naive and treated primary and secondary prevention patients with a high risk of a cardiovascular event.
  • collapse DIALOOG: Crestor in Patients With Diabetes Mellitus Type 2: Lowering of LDL-C Levels to New European Guidelines
  • collapse Crestor RAPID (The efficacy of RosuvAstatin for korean dyslipidemia PatIents with Diabetes)
  • collapse Study in High Risk Patients Switched From Higher Doses of Other Statins to Crestor on the Percentage of Patients Reaching the New LDL-C Target Goal
  • collapse SA-NXY-0013 Effects of cimetidine and probenecid on NXY-059
  • collapse CHANT (Cerebral Hemorrhage And NXY Treatment) A double-blind, randomized, placebo-controlled, parallel-group, multicenter, phase IIb study to assess the safety and tolerability of 72 hours intravenous infusion of NXY-059 in adult patients with acute intracerebral hemorrhge (ICH)
  • collapse Interaction between NXY-059 and furosemide? A PK/PD study of intravenous doses of the two drugs to healthy volunteers.
  • collapse A single-center phase I study in healthy, male volunteers, consisting of two separate randomized, double-blind, placebo controlled three-period cross-over sessions assessing the effect of NXY-059 (8 h i.v. infusion) on bleeding time, platelet aggregation and platelet adhesion as compared with that of desmopressin (10 min i.v. injection) and ASA (160 mg o.d. for three days) respectively
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