Clinical trial

Study Comparing Conversion to Sirolimus vs. Continued Use of Calcineurin…

NCT00038948 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed

Key facts

NCT number NCT00038948
Title Study Comparing Conversion to Sirolimus vs. Continued Use of Calcineurin Inhibitors in Kidney Transplant Recipients
Official title A Randomized, Open-label, Comparative Evaluation of Conversion From Calcineurin Inhibitors to Sirolimus Versus Continued Use of Calcineurin Inhibitors in Renal Allograft Recipients
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Renal Transplantation
Intervention type Drug
Interventions Sirolimus, tacrolimus, Cyclosporine A
Enrollment 830
Start date Jan 1, 2002
Primary completion May 1, 2008
Completion May 1, 2008
First posted Jun 7, 2002
Last update posted May 14, 2010

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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