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NCT00477542 · ClinicalTrials.gov registry record · Phase 1

A Phase I Trial of Myeloablative Conditioning w/ Clofarabine and HD Busulfan for Pts w/ Refractory Heme Malignancies Undergoing Allo PBSCT

A Phase 1 study, sponsored by Indiana University.

Completed
Registry status
Phase 1
Development phase
18
Enrollment target

NCT00477542 is a Phase 1 study that has completed, run by Indiana University. The registered enrollment target is 18 participants.

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The verdict

NCT00477542, a Phase 1 study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
Phase 1
Development phase
18 participants
Enrollment target

Study Summary

This is a phase trial to determine the maximum tolerated dose (MTD) of clofarabine in a combination with a myeloablative dose of busulfan. This is an initial step in developing a novel myeloablative preparative regimen for allogeneic hematopoietic stem cell transplantation (HSCT). While this phase I trial will initially develop the regimen in patients with refractory disease, it is expected that it will find its best application in patients with less advanced disease

Interventions

  • DRUG clofarabine

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2007-05
Est. Completion 2010-11
Phase Phase 1

Sponsor

Indiana University

890 total trials

What the Registry Record Tells You About NCT00477542

The ClinicalTrials.gov registry entry for NCT00477542 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.

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

NCT00477542 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00477542 about?

NCT00477542 is a clinical study titled "A Phase I Trial of Myeloablative Conditioning w/ Clofarabine and HD Busulfan for Pts w/ Refractory Heme Malignancies Undergoing Allo PBSCT". This is a phase trial to determine the maximum tolerated dose (MTD) of clofarabine in a combination with a myeloablative dose of busulfan. This is an initial step in developing a novel myeloablative preparative regimen for allogeneic hematopoietic stem cell transplantation (HSCT). While this phase I...

What is the current status of trial NCT00477542?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2007-05. Estimated completion is 2010-11.

What interventions are being tested in trial NCT00477542?

The interventions under investigation include: clofarabine (DRUG).

Who is sponsoring clinical trial NCT00477542?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.