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A two-year extension to a one-year, multicenter, partially blinded, double-dummy, randomized study to evaluate the efficacy and safety of FTY720 combined with reduced-dose or full-dose cyclosporine, USP [Modified] (Novartis Brand) and corticosteroids versus mycophenolate mofetil combined with full-dose cyclosporine, USP [Modified] (Novartis Brand) and corticosteroids, in de novo adult renal transplant recipients.

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Trial Profile

A two-year extension to a one-year, multicenter, partially blinded, double-dummy, randomized study to evaluate the efficacy and safety of FTY720 combined with reduced-dose or full-dose cyclosporine, USP [Modified] (Novartis Brand) and corticosteroids versus mycophenolate mofetil combined with full-dose cyclosporine, USP [Modified] (Novartis Brand) and corticosteroids, in de novo adult renal transplant recipients.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 01 Mar 2017

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At a glance

  • Drugs Fingolimod (Primary) ; Ciclosporin; Corticosteroids; Mycophenolate mofetil
  • Indications Renal transplant rejection
  • Focus Therapeutic Use
  • Sponsors Novartis

    • Most Recent Events

    • 01 Nov 2011 Actual end date (May 2006) added as reported by ClinicalTrials.gov.
    • 17 Dec 2005 New trial record.

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