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NCT00885820 · ClinicalTrials.gov registry record · Phase 4

Benefit of Early Protocol Biopsy and Treatment of Subclinical Rejection

A Phase 4 study, sponsored by Astellas Pharma.

Completed
Registry status
Phase 4
Development phase
240
Enrollment target

NCT00885820: Completed Phase 4 study, sponsored by Astellas Pharma.

NCT00885820 is a Phase 4 study that has completed, run by Astellas Pharma. The registered enrollment target is 240 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (54% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00885820, a Phase 4 study, has completed, sponsored by Astellas Pharma.

COMPLETED
Registry status
Phase 4
Development phase
240 participants
Enrollment target

Study Summary

This multicentre randomized, controlled trial (RCT) compared renal allograft histology and function in subjects treated with Tacrolimus + MMF + prednisone undergoing early protocol biopsies and treatment of subclinical rejection versus a non-protocol biopsy control group.

Interventions

  • DRUG Tacrolimus
  • DRUG MMF
  • DRUG Corticosteroids (Prednisone)

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2001-09
Est. Completion 2006-01
Phase Phase 4
Astellas Pharma

165 total trials

What the finished NCT00885820 record still lists

NCT00885820 is an interventional study that assigns participants to a tested intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (54% lower).

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

NCT00885820 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00885820 about?

NCT00885820 is a clinical study titled "Benefit of Early Protocol Biopsy and Treatment of Subclinical Rejection". This multicentre randomized, controlled trial (RCT) compared renal allograft histology and function in subjects treated with Tacrolimus + MMF + prednisone undergoing early protocol biopsies and treatment of subclinical rejection versus a non-protocol biopsy control group.

What is the current status of trial NCT00885820?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 240 participants. The study started on 2001-09. Estimated completion is 2006-01.

What interventions are being tested in trial NCT00885820?

The interventions under investigation include: Tacrolimus (DRUG), MMF (DRUG), Corticosteroids (Prednisone) (DRUG).

Who is sponsoring clinical trial NCT00885820?

This trial is sponsored by Astellas Pharma, which has 165 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00885820's enrollment target sits among peer trials

240 360th of 2000 higher than 1,635 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT00885820, the US trial registry maintained by the National Library of Medicine. NCT00885820 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.