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NCT00352976 · ClinicalTrials.gov registry record · Phase 2

TBI Dose De-escalation for Fanconi Anemia

A Phase 2 study, sponsored by Masonic Cancer Center, University of Minnesota.

Completed
Registry status
Phase 2
Development phase
83
Enrollment target

NCT00352976: Completed Phase 2 study, sponsored by Masonic Cancer Center, University of Minnesota.

NCT00352976 is a Phase 2 study that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 83 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00352976, a Phase 2 study, has completed, sponsored by Masonic Cancer Center, University of Minnesota.

COMPLETED
Registry status
Phase 2
Development phase
83 participants
Enrollment target

Study Summary

This is a single arm, total body irradiation (TBI) trial. All patients will be prescribed TBI 300 cGy with the goal of evaluating secondary endpoints.

Primary Outcome

Number of participant with neutrophil recovery. Neutrophil recovery is defined as absolute neutrophil count ≥500/µL for three consecutive days

Interventions

  • DRUG Cyclophosphamide
  • DRUG Fludarabine
  • DRUG Mycophenolate Mofetil
  • PROCEDURE Bone Marrow Transplantation
  • PROCEDURE Total Body Irradiation

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2006-05-18
Est. Completion 2020-10-09
Phase Phase 2

What the finished NCT00352976 record still lists

NCT00352976 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (38% lower).

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

NCT00352976 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00352976 about?

NCT00352976 is a clinical study titled "TBI Dose De-escalation for Fanconi Anemia". This is a single arm, total body irradiation (TBI) trial. All patients will be prescribed TBI 300 cGy with the goal of evaluating secondary endpoints.

What is the current status of trial NCT00352976?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 83 participants. The study started on 2006-05-18. Estimated completion is 2020-10-09.

What interventions are being tested in trial NCT00352976?

The interventions under investigation include: Cyclophosphamide (DRUG), Fludarabine (DRUG), Mycophenolate Mofetil (DRUG), Bone Marrow Transplantation (PROCEDURE), Total Body Irradiation (PROCEDURE).

Who is sponsoring clinical trial NCT00352976?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00352976's enrollment target sits among peer trials

83 828th of 2000 higher than 1,171 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 NCT00352976, the US trial registry maintained by the National Library of Medicine. NCT00352976 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.