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5, 6 or 7 year follow-up control after the SCHEDULE study (SCANDINAVIAN HEART TRANSPLANT EVEROLIMUS DE NOVO STUDY WITH EARLY CNI AVOIDANCE) Title of the original SCHEDULE study: A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®) and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant recipients can improve long-term renal function and slow down the progression of chronic allograft vasculopathy. (Protocol: CRAD001ANO02, EudraCT no.: 2009-013074-41)

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Trial Profile

5, 6 or 7 year follow-up control after the SCHEDULE study (SCANDINAVIAN HEART TRANSPLANT EVEROLIMUS DE NOVO STUDY WITH EARLY CNI AVOIDANCE) Title of the original SCHEDULE study: A controlled randomized open-label multicentre study evaluating if early initiation of everolimus (Certican®) and early elimination of cyclosporine (Sandimmun Neoral®) in de novo heart transplant recipients can improve long-term renal function and slow down the progression of chronic allograft vasculopathy. (Protocol: CRAD001ANO02, EudraCT no.: 2009-013074-41)

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 04 Oct 2019

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At a glance

  • Drugs Everolimus (Primary) ; Ciclosporin; Corticosteroid; Mycophenolate mofetil
  • Indications Heart transplant rejection
  • Focus Therapeutic Use
  • Sponsors Novartis Norge

    • Most Recent Events

    • 05 Feb 2018 Status changed from recruiting to completed.
    • 01 Feb 2018 This trial has been completed in Sweden (End date: 25 Sep 2017)
    • 29 Sep 2016 New trial record

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