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NCT00709592 · ClinicalTrials.gov registry record · Phase 2

Reduced Intensity Total Body Irradiation + Thymoglobulin Followed by Allogeneic PBSCT

A Phase 2 study, sponsored by Virginia Commonwealth University.

Completed
Registry status
Phase 2
Development phase
42
Enrollment target

NCT00709592: Completed Phase 2 study, sponsored by Virginia Commonwealth University.

NCT00709592 is a Phase 2 study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 42 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00709592, a Phase 2 study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
Phase 2
Development phase
42 participants
Enrollment target

Study Summary

One of two different doses of thymoglobulin will allow bone marrow engraftment with minimal Graft-versus-Host Disease and allow adequate immune response to allow the transplanted stem cells to replace the tumor cells.

Primary Outcome

A positive test result will indicate immune reconstitution, while a negative test results will indicate lack of immune reconstitution. Participants not done (ND) will be counted with the negative (Neg).

Interventions

  • RADIATION Total-Body Irradiation
  • DRUG Mycophenolate Mofetil
  • DRUG Tacrolimus
  • BIOLOGICAL Thymoglobulin
  • PROCEDURE Allogeneic PBSCT or BMT

Trial Details

FieldValue
Enrollment Target 42 participants
Start Date 2008-07-21
Est. Completion 2017-06-28
Phase Phase 2
Virginia Commonwealth University

558 total trials

What the finished NCT00709592 record still lists

NCT00709592 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 42 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (68% lower).

The record links to 0 conditions, and to 5 interventions - of which Total-Body Irradiation is the first listed.

NCT00709592 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00709592 about?

NCT00709592 is a clinical study titled "Reduced Intensity Total Body Irradiation + Thymoglobulin Followed by Allogeneic PBSCT". One of two different doses of thymoglobulin will allow bone marrow engraftment with minimal Graft-versus-Host Disease and allow adequate immune response to allow the transplanted stem cells to replace the tumor cells.

What is the current status of trial NCT00709592?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 42 participants. The study started on 2008-07-21. Estimated completion is 2017-06-28.

What interventions are being tested in trial NCT00709592?

The interventions under investigation include: Total-Body Irradiation (RADIATION), Mycophenolate Mofetil (DRUG), Tacrolimus (DRUG), Thymoglobulin (BIOLOGICAL), Allogeneic PBSCT or BMT (PROCEDURE).

Who is sponsoring clinical trial NCT00709592?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00709592's enrollment target sits among peer trials

42 1339th of 2000 higher than 649 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00709592, the US trial registry maintained by the National Library of Medicine. NCT00709592 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.