Status:

COMPLETED

Ranolazine SR in Patients With Chronic Angina Who Remain Symptomatic Despite Maximal Treatment With Amlodipine

Lead Sponsor:

Gilead Sciences

Conditions:

Angina

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

The study will be a multi-national, double-blind, randomized, placebo-controlled, parallel group study to evaluate the effectiveness of ranolazine (1000 mg twice daily) in approximately 500 patients w...

Eligibility Criteria

Inclusion

  • Eligible patients must have a diagnosis of chronic angina, with documented evidence of coronary artery disease or prior myocardial infarction, in addition to other study entry criteria. Prior to entering the study, patients will be required to have had at least two weeks of treatment with amlodipine 10 mg daily, with the discontinuation of all other anti-anginal therapy for the duration of the study.

Exclusion

    Key Trial Info

    Start Date :

    August 1 2004

    Trial Type :

    INTERVENTIONAL

    End Date :

    February 1 2005

    Estimated Enrollment :

    500 Patients enrolled

    Trial Details

    Trial ID

    NCT00091429

    Start Date

    August 1 2004

    End Date

    February 1 2005

    Last Update

    November 26 2009

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