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NCT00320606 · ClinicalTrials.gov registry record · Phase 1

Withdrawal of Immunosuppression in Pediatric Liver Transplant Recipients

A Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 1
Development phase
20
Enrollment target

NCT00320606: Completed Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT00320606 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00320606, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
20 participants
Enrollment target

Study Summary

Antirejection medicines, also known as immunosuppressive drugs, are prescribed to organ transplant recipients to prevent their bodies from rejecting the new organ. Long-term use of these drugs places transplant recipients at higher risk of serious infections and certain types of cancer. The purpose of this study is to determine whether immunosuppressive drugs can be safely withdrawn over a minimum of 9 months from children who received liver transplants at least 4 years ago.

Primary Outcome

Participants were considered successfully withdrawn from immunosuppression if they remained off immunosuppression for at least one year with normal allograft function.

Interventions

  • DRUG Immunosuppression Withdrawal

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2006-06-05
Est. Completion 2017-03-13
Phase Phase 1

What the finished NCT00320606 record still lists

NCT00320606 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).

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

NCT00320606 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00320606 about?

NCT00320606 is a clinical study titled "Withdrawal of Immunosuppression in Pediatric Liver Transplant Recipients". Antirejection medicines, also known as immunosuppressive drugs, are prescribed to organ transplant recipients to prevent their bodies from rejecting the new organ. Long-term use of these drugs places transplant recipients at higher risk of serious infections and certain types of cancer. The purpose ...

What is the current status of trial NCT00320606?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2006-06-05. Estimated completion is 2017-03-13.

What interventions are being tested in trial NCT00320606?

The interventions under investigation include: Immunosuppression Withdrawal (DRUG).

Who is sponsoring clinical trial NCT00320606?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00320606's enrollment target sits among peer trials

20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00320606, the US trial registry maintained by the National Library of Medicine. NCT00320606 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.