Status:

COMPLETED

48-wk Open Label Phase IIIb to Evaluate Efficacy and Safety

Lead Sponsor:

AstraZeneca

Conditions:

Dyslipidaemia

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The purpose of this study is to assess the efficacy and safety of rosuvastatin in reducing low density lipoprotein cholesterol levels to internationally recognised goals in subjects with dyslipidaemia...

Eligibility Criteria

Inclusion

  • Fasting low density lipoprotein level as defined by the protocol.
  • Fasting triglyceride level as defined by the protocol.

Exclusion

  • The use of lipid lowering drugs or dietary supplements after Visit 1.
  • Active arterial disease eg Unstable angina, or recent arterial surgery.
  • Blood lipid levels above the limits defined in the protocol.
  • Uncontrolled hypertension, hypothyroidism, alcohol or drug abuse.

Key Trial Info

Start Date :

February 1 2002

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

November 1 2004

Estimated Enrollment :

1500 Patients enrolled

Trial Details

Trial ID

NCT00654602

Start Date

February 1 2002

End Date

November 1 2004

Last Update

May 28 2009

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48-wk Open Label Phase IIIb to Evaluate Efficacy and Safety | DecenTrialz