Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00137345 · ClinicalTrials.gov registry record · Phase 3

Study Comparing Sirolimus With Cyclosporine in a Calcineurin Inhibitor (CNI)-Free Regimen in Kidney Transplant Recipients

A Phase 3 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Terminated
Registry status
Phase 3
Development phase
500
Enrollment target

NCT00137345 is a Phase 3 study that was terminated before completion, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 500 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00137345, a Phase 3 study, was terminated before completion, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

TERMINATED
Registry status
Phase 3
Development phase
500 participants
Enrollment target

Study Summary

The purpose of this study is to determine if one drug is superior to another with regard to safety and the preservation of renal function after a kidney transplant.

Interventions

  • DRUG sirolimus

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2005-06
Est. Completion 2006-08
Phase Phase 3

What the Registry Record Tells You About NCT00137345

The ClinicalTrials.gov registry entry for NCT00137345 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which sirolimus is the first listed.

NCT00137345 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00137345 about?

NCT00137345 is a clinical study titled "Study Comparing Sirolimus With Cyclosporine in a Calcineurin Inhibitor (CNI)-Free Regimen in Kidney Transplant Recipients". The purpose of this study is to determine if one drug is superior to another with regard to safety and the preservation of renal function after a kidney transplant.

What is the current status of trial NCT00137345?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 500 participants. The study started on 2005-06. Estimated completion is 2006-08.

What interventions are being tested in trial NCT00137345?

The interventions under investigation include: sirolimus (DRUG).

Who is sponsoring clinical trial NCT00137345?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.