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A 12-month, Prospective, Randomized, Dual Center, Open Label Pilot Study to Evaluate the Safety and Efficacy of Myfortic (R) (Mycophenolic Acid) Loading Regimens in Combination With Thymoglobulin (R) [Anti-thymocyte Globulin (Rabbit)] or Simulect (R) (Basiliximab) Induction and Prograf (R) (Tacrolimus) in Early Corticosteroid Withdrawal

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Trial Profile

A 12-month, Prospective, Randomized, Dual Center, Open Label Pilot Study to Evaluate the Safety and Efficacy of Myfortic (R) (Mycophenolic Acid) Loading Regimens in Combination With Thymoglobulin (R) [Anti-thymocyte Globulin (Rabbit)] or Simulect (R) (Basiliximab) Induction and Prograf (R) (Tacrolimus) in Early Corticosteroid Withdrawal

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 07 Nov 2021

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At a glance

  • Drugs Mycophenolate sodium (Primary) ; Antithymocyte globulin; Basiliximab; Tacrolimus
  • Indications Renal transplant rejection
  • Focus Therapeutic Use

    • Most Recent Events

    • 29 May 2014 According to the ClinicalTrials.gov record, status changed from recruiting to completed.
    • 18 Jun 2012 Planned end date changed from 1 May 2013 to 1 May 2014 as reported by ClinicalTrials.gov.
    • 18 Apr 2011 New trial record

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