Clinical trial

Reduction in the Risk of Rejection by Mycophenolate Mofetil Dose Adjustment in…

NCT00456235 · University Hospital, Limoges, Other · Completed

Key facts

NCT number NCT00456235
Title Reduction in the Risk of Rejection by Mycophenolate Mofetil Dose Adjustment in Liver Transplant Patients With Side Effects Caused by the Calcineurine Inhibitors
Official title Interruption of the Calcineurine Inhibitors (ICN) and Introduction of Mycophenolate Mofetil (MMF) in Liver Transplant Patients With Side Effects Due to ICN: Study of the Reduction of the Risks of Rejection by Mycophenolate Mofetil Therapeutic Drug Monitoring
Acronym MONOCEPT
Lead sponsor University Hospital, Limoges, Other
Status Completed
Phase Phase 4
Study type Interventional
Conditions Liver Transplantation
Intervention type Drug
Interventions Mycophénolate Mofétil, Ciclosporine A, Tacrolimus
Enrollment 92
Start date Sep 1, 2006
Primary completion Sep 1, 2009
Completion Sep 1, 2011
First posted Apr 4, 2007
Last update posted Apr 17, 2013
Countries France

At a glance

  • 10–99 Study sites
  • No 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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