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

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, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

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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

Why NCT00137345 stopped before completion

NCT00137345 is an interventional study that assigns participants to a tested intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (35% lower).

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

NCT00137345 does not publish any study locations in the registry export this page uses.

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.

How this trial's enrollment target compares

Where NCT00137345's enrollment target sits among peer trials

500 744th of 2000 higher than 1,226 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00137345, the US trial registry maintained by the National Library of Medicine. NCT00137345 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.