Clinical trial

Study Evaluating of Calcineurin Inhibitors Versus Sirolimus in Renal Allograft…

NCT00452361 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Terminated

Key facts

NCT number NCT00452361
Title Study Evaluating of Calcineurin Inhibitors Versus Sirolimus in Renal Allograft Recipient
Official title A Randomized, Open-label, Comparative Evaluation of Conversion From Calcineurin Inhibitors to Sirolimus Versus Continued Use of Calcineurin Inhibitors in Renal Allograft Recipient
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Terminated
Phase Phase 4
Study type Interventional
Conditions Kidney Transplantation
Intervention type Drug
Interventions Sirolimus+MMF or MPS or AZA+Steroid, Calcineurin Inhibitors (either cyclosporine or tacrolimus)+MMF or MPS or AZA+Steroid
Enrollment 31
Start date Apr 1, 2007
Primary completion Aug 1, 2008
Completion Aug 1, 2008
First posted Mar 27, 2007
Last update posted Sep 3, 2012
Countries Taiwan

At a glance

  • 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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