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NCT00990249 · ClinicalTrials.gov registry record · Phase 2

Busulfan Plus Clofarabine Followed by Allogeneic Hematopoietic Stem Cell Transplantation

A Phase 2 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 2
Development phase
120
Enrollment target

NCT00990249: Completed Phase 2 study, sponsored by M.D. Anderson Cancer Center.

NCT00990249 is a Phase 2 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 120 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00990249, a Phase 2 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

The goal of this clinical research study is to test the safety of giving clofarabine in combination with busulfan, followed by an allogeneic (from a donor) stem cell transplant, in patients with advanced leukemia or lymphoma.

Primary Outcome

NRM was defined as death from any cause other than disease progression or relapse and reported as percentage of participant deaths. Treatment related deaths after transplant are defined either by deaths which could not be attributed to disease relapse or progression or by deaths without previous relapse or progression. For TRM at day 100, Bayesian method of Thall, Simon, and Estey used to perform interim monitoring.

Interventions

  • DRUG Busulfan
  • DRUG Thymoglobulin
  • DRUG Clofarabine
  • PROCEDURE Stem Cell Transplant

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2009-10
Est. Completion 2016-05
Phase Phase 2
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00990249 record still lists

NCT00990249 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower).

The record links to 0 conditions, and to 4 interventions - of which Busulfan is the first listed.

NCT00990249 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00990249 about?

NCT00990249 is a clinical study titled "Busulfan Plus Clofarabine Followed by Allogeneic Hematopoietic Stem Cell Transplantation". The goal of this clinical research study is to test the safety of giving clofarabine in combination with busulfan, followed by an allogeneic (from a donor) stem cell transplant, in patients with advanced leukemia or lymphoma.

What is the current status of trial NCT00990249?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2009-10. Estimated completion is 2016-05.

What interventions are being tested in trial NCT00990249?

The interventions under investigation include: Busulfan (DRUG), Thymoglobulin (DRUG), Clofarabine (DRUG), Stem Cell Transplant (PROCEDURE).

Who is sponsoring clinical trial NCT00990249?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00990249's enrollment target sits among peer trials

120 569th of 2000 higher than 1,383 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 NCT00990249, the US trial registry maintained by the National Library of Medicine. NCT00990249 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.