Clinical trial

Evaluation of the Therapeutic Benefit of an Initial Intensified Dosing Regimen…

NCT00419926 · Novartis, Industry · Completed

Key facts

NCT number NCT00419926
Title Evaluation of the Therapeutic Benefit of an Initial Intensified Dosing Regimen of Mycophenolate Sodium Versus a Standard Regimen in Renal Transplant Patients
Official title A Randomized, Multicenter, Parallel-group, Open-label Study to Evaluate the Therapeutic Benefit of an Initially Intensified Dosing Regimen of Mycophenolate Sodium Versus a Standard Dosing Regimen, in Combination With Cyclosporine and Corticosteroids in de Novo Renal Transplant Patients
Lead sponsor Novartis, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Kidney Transplantation
Intervention type Drug
Interventions Enteric-coated mycophenolate sodium (Myfortic), Cyclosporine (Neoral), Prednisone
Enrollment 313
Start date Dec 1, 2006
Primary completion Jun 1, 2009
Completion Jun 1, 2009
First posted Jan 9, 2007
Last update posted Mar 1, 2011
Countries Switzerland

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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