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NCT01473732 · ClinicalTrials.gov registry record · NA

Mechanisms and Treatment of Chronic Allograft Injury (CAI) Due to Calcineurin Inhibitor (CNI) Toxicity

A NA study, sponsored by Montefiore Medical Center.

Terminated
Registry status
NA
Development phase
2
Enrollment target

NCT01473732: Clinical Trial NA study, sponsored by Montefiore Medical Center.

NCT01473732 is a NA study that was terminated before completion, run by Montefiore Medical Center. The registered enrollment target is 2 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01473732, a NA study, was terminated before completion, sponsored by Montefiore Medical Center.

TERMINATED
Registry status
NA
Development phase
2 participants
Enrollment target

Study Summary

The purpose of this study is to find out how well the current drug regimen (including low Prograf dose and Myfortic, which is usually recommended to prevent any further deterioration in the kidney function) works and how safe it is when compared to a combination of Zortress and Myfortic in patients with chronic kidney injury associated with Prograf or Neoral use.

Primary Outcome

Estimated glomerular filtration rate (eGFR) indicates kidney function. Normal eGFR value for healthy is 80-120ml/min. For transplants, it is expected to be 60-80 ml/min.

Interventions

  • DRUG Everolimus
  • DRUG Tacrolimus
  • DRUG Mycophenolic acid

Trial Details

FieldValue
Enrollment Target 2 participants
Start Date 2012-03
Est. Completion 2012-08
Phase NA
Montefiore Medical Center

345 total trials

Why NCT01473732 stopped before completion

NCT01473732 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 2 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 3 interventions - of which Everolimus is the first listed.

NCT01473732 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01473732 about?

NCT01473732 is a clinical study titled "Mechanisms and Treatment of Chronic Allograft Injury (CAI) Due to Calcineurin Inhibitor (CNI) Toxicity". The purpose of this study is to find out how well the current drug regimen (including low Prograf dose and Myfortic, which is usually recommended to prevent any further deterioration in the kidney function) works and how safe it is when compared to a combination of Zortress and Myfortic in patients ...

What is the current status of trial NCT01473732?

This trial is currently terminated. It is a NA study. The enrollment target is 2 participants. The study started on 2012-03. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01473732?

The interventions under investigation include: Everolimus (DRUG), Tacrolimus (DRUG), Mycophenolic acid (DRUG).

Who is sponsoring clinical trial NCT01473732?

This trial is sponsored by Montefiore Medical Center, which has 345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01473732's enrollment target sits among peer trials

2 1997th of 2000 the lowest of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT01473732, the US trial registry maintained by the National Library of Medicine. NCT01473732 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.